Surface proteins of Leptospira

ABSTRACT

The invention relates to Leptospiral surface proteins, and the nucleic acid molecules which encode them. Various uses are described, including immunoprophylactic, diagnostic and therapeutic methods.

RELATED APPLICATION

[0001] This application claims priority of application Ser. No. 60/360,566, filed Feb. 28, 2002, incorporated by reference in its entirety.

FIELD OF THE INVENTION

[0002] This invention relates to membrane associated proteins of Leptospira bacteria, Leptospira Copenhageni in particular. The proteins are useful both therapeutically, as, e.g., antisera, immunoprophylactically, as vaccines, as well as diagnostically. They can be used, for example, to detect antibodies in samples taken from subjects suspected of being infected, and also to generate antibodies which can then be used to detect the proteins, epitopic portions of the proteins, as well as the bacteria per se. Also a feature of the invention are nucleic acid molecules encoding these proteins, methods for purifying them, as well as various applications thereof.

BACKGROUND AND PRIOR ART

[0003] Leptospira is a genus of bacteria which is a member of the Spirochetes family. Other members of this family are Borrelia and Treponema. All three genuses are characterized by mobility, and a helical shape. All members of the family cause disease in animals, including humans, livestock, domesticated animals, and wild animals. For example, Borrelia is the causative agent for Lyme disease. Other diseases caused by Spirochetes include relapsing fever, syphilis and yaws.

[0004] Leptospira genus consists of a genetically diverse group of 12 species, eight of which are pathogenic, and four of which are non-pathogenic, and saprophytic. See Faine, et al., Leptospira and Leptospirosis (2^(nd) edition, 1999, Melbourne, Australia, MediSci); Farr, Clin. Infect. Dis 21:1-8 (1995). Levett, Clin. Microbiol Rev. 14:296-326 (2001), incorporated by reference. There are over 200 known pathogenic serovars of Leptospira. It is hypothesized that structural heterogeneity in lypopolysacchacide structure accounts for this. See, Levett, supra.

[0005] Leptospirosis, the disease caused by Leptospira, is zoonotic. Transmission to humans results from contact with domestic or wild animal reservoirs, or via contact with animal urine. Infected individuals show a wide spectrum of clinical manifestations in the early phases of the illness including fever, headache, chills and severe myalgia. In 5-15% of the clinical infections, severe multisystem complications result, including jaundice, renal failure and hemorrhaging. See Farr, supra, Faine, et al., supra. Severe leptospirosis has a mortality rate of 5-40%.

[0006] There is a large spectrum of animal species which serve as reservoirs for the bacteria. As a result, human leptospirosis is found throughout the world, and is considered to be the most widespread zoonotic disease. High risk groups include military personnel, farmers, miners, sewage and waste removal workers, veterinarians and abattoir workers. See, in this regard, Levett, supra, Faine, et al., supra. New patterns of transmission of the disease have emerged; however, emphasizing the public health issues associated with this disease. In “developed” countries outbreaks have been associated with recreational diseases, such as white water rafters in Costa Rica, and sporting events involving extensive outdoor activity, such as triathlons and “Eco-challenges.” See, e.g., Levett, supra; Jackson, Pediatr. Infect. Dis. J 12:48-54 (1993); Center For Disease Control and Prevention: Outbreak of leptospirosis among white water rafters in Costa Rica (1997); Update: Leptospirosis and Unexplained Acute febrile illness among athletes participating in triathlons: Illinois and Wisconsin (1998). Update: Outbreak of Acute Illness Among Athletes Participating in Eco-Challenge—Sahah 2000—Borneo, Malaysia (2000). Underlying conditions associated with poverty have led to large, urban, epidemics of leptospirosis in Brazil and other countries, resulting in high mortality rates. See Lomor, et al., Infect. Dis. Clin. North Am 14:23-39 (2000); Ko, et al., Lancet 354:820-5 (1999).

[0007] Leptospirosis is a major issue in agriculture as well, due to its association with livestock and domestic animals. Among the manifestations of animal leptospirosis are spontaneous abortions, still births, infertility, failure to thrive, reduced milk production, and high fatality rates in diverse species such as cows, pigs, sheep, goats, horses and dogs. See Faine, et al., supra. Other manifestations of the disease are chronic infection, and shedding of pathogenic leptospires. Standard approaches to controlling this include international and national quarantines in the animal husbandry industry, with negative economic ramifications.

[0008] Clearly, there is a need to control leptospirosis; however, efforts have been hindered due to a lack of effective approaches. Long term survival of pathogenic leptospires in soil and water, as well as the abundance of animal reservoirs support long term survival of the pathogen so eradication is not a viable option. Hence, efforts have turned to approaches based upon vaccines.

[0009] Currently, available vaccines are based upon inactivated whole cell, or membrane preparations of pathogenic bacteria. These appear to induce protective responses via antibody induction. See Levett, supra, Faine, et al, supra. These vaccines do not produce long term protection against infection, and they do not confer cross protective immunity against serovars not included in the vaccines used. The number of serovars possible, and the cost of multicomponent serovar vaccines have thwarted development in this area.

[0010] A key mechanism in the pathogenesis of leptospirosis, as in other spirochetal diseases (such as Lyme disease and syphilis), is the ability of the pathogen to disseminate widely in the host during the early stage of infection. See Faine, et al., supra. It is presumed that surface associated leptospiral proteins, mediate interactions which facilitate entry and dissemination through host tissues. Virulence factors associated with the surface of the bacteria serve as vaccine candidates, in that any immune or other protective response would block dissemination in the host. Another important aspect of surface associated proteins is that they are, literally, “surface-associated,” rendering them accessible to immune attack. Protective mechanisms associated with such surface associated proteins include antibody-dependent phagacytosis, and complement-mediated killing.

[0011] It would be desirable to have pure, or substantially pure Leptospira surface associated proteins available. Production of such proteins, in recombinant form, for example is cost effective, and provides a method to screen proteins to determine sub-unit or epitopic fragment based vaccines. Further, availability of recombinant proteins permits one to determine which proteins are conserved, especially among different pathogenic Leptospira, to determine which are the most suitable, cross-serovar vaccines.

[0012] There have been difficulties in identifying surface associated Leptospira proteins, using conventional biochemical and molecular biological methods. The genome of the spirochete Borrelia burgdorferi has been analyzed, and more than 100 surface associated lepoproteins were identified. The large size of the Leptospira genome (˜4.6 Mb), and its complex life cycle suggest that a far greater number of surface associated proteins will be found. Using standard membrane extraction, isolation, and purification techniques, less than 10 Leptospira surface associated proteins have been identified and characterized. See Haake, et al., Infect. Immun 66:1579-1587 (1998); Haake, et al., Infect. Immun. 6572-82 (1999); Haake, et al., Infect. Immun 68:2276-2285 (2000); Shang, et al., Infect. Immun 63:3174-3181 (1995); Shang, et al., Infect. Immun 64:2232-30 (1996). Also see U.S. Pat. Nos. 5,091,301; 5,643,754; 5,638,757; 5,824,321; 6,140,083; 6,262,235; 6,306,623; and 6,308,641. All of these articles and patents are incorporated by reference. While Haake, et al., Infect. Immun 67:6572-82 (1999), describe immunization with recombinant protein L1pL32, OmpL1 and L1pL41 but, the response was not complete. None of these reference identify virulence associated proteins.

[0013] As has been pointed out, supra, the Leptospira genome is large. As a result, technical difficulties have prevented meaningful results in identifying surface associated proteins; however, the emerging field of bioinformatics has placed extremely powerful and valuable tools in the hands of those involved in Leptospiral research.

[0014] Via application of the techniques described supra, the inventors have discovered further Leptospira surface associated proteins useful in vaccine production, as well as in production of diagnostic kits for use in determining presence, onset, or decrease in Leptospiral infection. These, and other aspects of the invention will be clear from the disclosure which follows.

BRIEF DESCRIPTION OF THE FIGURES

[0015] FIGS. 1-22 inclusive, present data obtained from Western Blotting experiments, using the recombinant proteins of the invention. In all figures, control rat serum, and serum from rats that had been immunized with Leptospira, and control human sera as well as sera from patients diagnosed as suffering from Leptospirosis were used. FIG. 1 shows work done with the protein of SEQ ID NO: 2 & 4, FIG. 2 with SEQ ID NO: 6 & 8, and so forth.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS EXAMPLE 1

[0016] A strain of Leptospira, referred to as “Fiocruz L1-30,” was used. The strain was isolated from a patient with severe leptospirosis, contracted during an epidemic in 1996. See Ko, et al., Lancet 354:820-5 (1999), incorporated by reference. Leptospires were detected during dark field microscopy examination of a culture of tween-albumin media that had been inoculated with patient blood, following “Guidelines for the Control of Leptospirosis.” WHO Offset Publ. (1982) incorporated by reference. The strain was identified as Leptospira interrogans, serovar Copenhageni, via biochemical and sera typing analysis. See Ko, et al., supra, Barocchi, et al., J. Clin. Microbiol 39:191-195 (2001). A culture of the organism was then prepared in media with 10% glycerol, and stored at −70° C. Virulence capacity was determined by inoculating 28 day old weaning hamsters. Kidneys were removed from anesthetized animals, approximately 7 days after infection, macerated and were used to inoculate Tween-albumin media. Any cultures for which growth was detected were used to infect additional hamsters, as part of a second passage step. In all, three passage steps were performed. Isolates from the final passage were used to prepare large scale, two liter cultures, again in Tween albumin media. Following centrifugation (10,000×g for 20 minutes), pellets were stored at −70° C., prior to use in DNA purification steps. The genomic DNA was extracted using standard methods, as set forth in, e.g., Sambrook and Maniatis, Molecular Cloning: A Laboratory Manual (2^(nd) edition, Cold Spring Harbor, 1989).

[0017] Once the genomic DNA was isolated, it was partially digested with MboI, in order to generate fragments which ranged from 30 to 60 kilobase pairs. These were cloned into a cosmid vector “Lawrist 4,” described by Hanke, et al., Biotechniques 21(4):686-8 and 690-3 (1996), incorporated by reference to produce a cosmid library. Any dephosphorylated DNA fragments were ligated to the cosmid vector, in the presence of T4 DNA ligase. The resulting, recombinant DNA was then packed into phage particles, using a commercially available product, and was then transfected into E. coli DH5*. Transfected cells were plated onto solid, Luria-Bertani medium supplemented with kanamycin, and were grown, overnight, at 37° C.

[0018] Following culture, the transfectants were used in a shotgun library construction protocol. To elaborate, genomic DNA was purified, in accordance with Fleischmann, et al., Science 269:496-512 (1995), incorporated by reference, and the purified DNA was sheared into fragments via nebulization.

[0019] The resulting fragments were repaired by end filling, using the Klenow fragment of E. coli DNA polymerase, or phage T7 DNA polymerase, or both, before ligation into the SmaI BAP site of pUC18. The resulting, recombinant DNA was transformed into E. coli DH10B cells, via electroporation. The transformants were plated, on Luria-Bertani agar medium containing ampicillin, and grown overnight at 37° C.

[0020] Single bacterial colonies resulting from the culture were inoculated in 96 well microtiter plates containing nutrient broth and ampicillin. These were grown, overnight, with shaking, at 37° C. DNA was purified via standard alkaline lysis, with one modification. Specifically, at the end of the procedure, supernatant was passed through a multi-screen filter prior to precipitation. Precipitated DNA was resuspended in water, and used as described in the following example.

EXAMPLE 2

[0021] The purified DNA described in example 1 was sequenced, using commercially available reagents, and well known methods.

[0022] Specifically, commercially available products were used to carry out Taq dye deoxy terminator cycle sequencing reactions, using M13 reverse and forward matching primers, which flanked the inserts of the clones. Reaction products were analyzed on a commercially available genetic analyzer.

[0023] There were a total of 289,963 shotgun genomic sequences. Open reading frames were obtained from these, and assembled using phred/phrap software, as described by Ewing, et al., Genome Res 8(3):186-194 (1998) incorporated by reference. The assembly yielded 2,042 contigs. The “Glimmer” program of Delcher, et al., Nucl. Acids Res 27:4636-4641 (1999), incorporated by reference, was applied to the contigs, and yielded 5826 putative open reading frames. Each of these ORFs contained at least 90 base pairs, and overlapped other ORFs by 30 base pairs, or 10% of the ORF size, at most. Any ORFs with “N” or “X,” which indicated either poor quality, or repetitive regions were discarded. The “PSORT” program described by Nakai, et al., Proteins: Structure, Function and Genetics 11:95-110 (1991), incorporated by reference, was used to predict protein location within the bacterium. Any ORF, with a PSORT score of 0.1 or more (outer membrane or periplasmic space localization), were considered to be potentially useful.

[0024] Protein coding genes were identified using known algorithms GeneMark and Glimmer, as described by Delcher, et al., Nucl. Acids Res. 27:4636-4641 (1999), incorporated by reference, after which the “PSORT” program, described by Nakai, et al., Proteins: Structure, Function and Genetics 11:95-110 (1991), incorporated by reference, was used to predict protein localization within the bacterium. The sequences chosen for further analysis were those which the program predicted to encode surface associated proteins. Such proteins are ideal candidates for generation of antibodies.

[0025] Once the relevant nucleotide sequences were identified, protocols were developed to amplify them for further work.

[0026] In each case, a pair of oligonucleotide primers were developed to hybridize specifically to the target sequence of interest. In general, primers from 18-28 nucleotides long were used. In each case, the forward primer was then modified to add the sequence “CACC” at the 5′ end. This facilitates directional cloning in the vector used. As a general principle, the primers were designed to hybridize from 10-25 amino acids away from the start codon, so as to avoid hydrophobic regions that are characteristic of signal peptide sequences. The primer sequences follow TABLE 1 Oligonucleotide primer sequences employed to amplify the target nucleic sequences by PCR methodology. Molecular weights are from the recombinant proteins obtained in E. coli expression systems. Molecular Weight (KDa) Primers LpL53 53.8 LpL53F: CACCACCAATGTGTTTGGTATAGCG LpL53R: CAGCGTTTTGTGATAAAATTAAC OMPL55 53.8 OMPL55F: CACCGATGCTTACTACGGACTGGATG OMPL55R: CAGGAGTGTGATCGAGCTTG OMPL16 15.9 OMPL16F: CACCCCGTGTTCTTTTGGTTTAGAT OMPL16R: TTCCAACAAATCGAATCATCT OMPL31 32 OMPL31F: CACCAAGAAGGATTCCAACGATGATG OMPL31R: TCTCCTGCTTGACAGCCGAC OMPL15 15.2 OMPL15F: CACCATGCGTGCTGTCAGTAGAGAAAC OMPL15R: GTCGACATTGGCAGAATTTACG OMPL20 21.2 OMPL20F: CACCTTTGCACAATCCAAAGAGAAATG OMPL20R: TCATTTCCGAACCGGATGAC LpL23 18.5 LpL23F: ACCATGGGATCCGCTCTTTTGGTTGATCCAGAG LpL23R: GAATTCCTAACAACCAGGACCTTCACAT LpL40 39 LpL40F: ACCATGGGACTCGAGACGCCTCCTCCTAAAGATCC LpL40R: CTCCATGGTCATTTCAAAACTTCTAGGGGGC LpL22 22.8 LpL22F: CACCCCTTCGAGGTTGGAAATCG LpL22R: AATCGATGGATCACGTTACG OMPL17 18.4 OMPL17F: CACCAAACCTGGATATGGAATGGC OMPL17R: TACAGAGGTAGAAGCGTTAGAAG OMPL30 29.2 OMPL30F: CACCAATCGACTTTTCACTGAGTTTCTT OMPL30R: CGAAAGTATCAAGAAGAACCGTA OMPL27 27.5 OMPL27F: CACCCAGGAAACGGAAAACGCTAA OMPL27R: CTTATTGTTTGCCGTAGGTTTC OMPL21 21.9 OMPL21F: CACCATGGGCGCTTTTAATCGG OMPL21R: CGGAACTAGGGAACTTTTCAAC OMPL22 20.6 OMPL22F: CACCATCATTCCTTCGGGAAGTGAC OMPL22R: CCATTCTCTGTTGTTTGATCCC MPL17 15.4 MPL17F: CACCGAAAGTCCCGTAAGGTTCAAA MPL17R: TGCAGGAGTTCCCACATTTTA MPL21 31.9 MPL21F: CACCACGTCTCAAAGTTACGCTTCAG MPL21R: TTCTCACCATCCAGCTCGG OMPAL21 20.6 OMPAL21F: CACCGAGCCTTCAACGCAAGAGCAA OMPAL21R: AACGTAAGACGTTGAGTTGCCACA OMPL63 64.3 OMPL63F: CACCACGATGATTCAGCCTACTTGG OMPL63R: GAAGTAGAACCGGAAGATTTATTT OMPL14 18.6 OMPL14F: CACCGGATGCAAACAAGATCCAGTAG OMPL14R: GAAACGCCACTAAGTTAGATCAC MPL36 35.1 MPL36F: CACCACGTCTTGTGCGTCGGTAGAG MPL36R: CCAAGTATTCTATTTATACGTCCGAG MPL39 30.8 MPL39F: CACCTCAGTAACTACTGGTCAGTGTAATG MPL39R: CACGTGTTAGTTCTTTGGTTG MPL40 43.2 MPL40F: CACCTTGTTTTTAAAAAAAAGGAAAGC MPL40R: AACTAAGGAACCGGAGTTGC MPL21 18.6 MPL21F: CACCGACATGCTTCCTACTTATTCCC MPL21R: CGCTAAAAGTATCACAATGGTAA

[0027] The amplification was carried out by combining template DNA (1.0 ng), nucleotide triphosphates (0.4 mM), Pfx polymerase (0.5 units, taken from a stock solution of 1 unit/μl), and 0.2 μM primers, at a pH of 8.0. The total reaction volume was 50 μl.

[0028] PCR was then carried out in a thermocycler, where the DNA denaturation step was carried out for 3 minutes at 94° C., followed by primer-DNA template annealing at 55° C., for 20 seconds, and nucleotide polymerization for 4 minutes at 68° C. This cycle was repeated, 45 times, except that in the repeats, denaturation was for 20 seconds.

[0029] Following amplification, the sequences were cloned into a commercially available vector, “pENTR.TOPO.” This vector includes a kanamycin resistance sequence useful in E. coli selection a pUC ORI, two “attL1” and “attL2” sites for site-specific recombination, and a TOPO cloning site for directional cloning of blunt end PCR products. Specifically, this is the sequence “CCCTT”, which serves as a topoisomerase I binding site.

[0030] Cloning was carried out according to manufacturer's instructions, which call for 15 ng of the PCR product, and 5 ng of pENTR.TOPO vector, in 5 mM Tris buffer, pH 7.4, at a total volume of 10 μl. The reaction proceeded for 10 minutes, at room temperature, i.e., about 25° C.

[0031] Positive clones were obtained via culture in kanamycin containing Luria Broth.

[0032] Following the reaction, the PCR products were integrated into the pENTR.TOPO vector, and were transferred to specific expression vectors very easily, via reaction at the forementioned attR1 and attR2 sites, in the presence of LR Clonase.

[0033] Expression was facilitated by use of an expression vector derived from T7, the commercially available pDEST17 vector. This vector includes an ORI, a promoter sequence to facilitate transcription of inserted sequences, a ribosomal binding site, and an ATG start codon.

[0034] In the practice of the invention, 2 μl of the cloning mixture described supra, 15 ng of pDEST17, & 4 μl of LR Clonase enzyme mix were combined in Tris-EDTA (10MM Tris-HCl, 0.1 mM EDTA) buffer, at pH 8, for 60 minutes, at room temperature. After 60 minutes, proteinase K (4 μg) was added for 30 minutes, at 37° C., to inactivate enzymes. Positive clones were isolated from Luria Broth agar plates, which contained 20 μg/ml of ampicillin. DNA sequences, when cloned, included a sequence encoding six His residues, at the N terminus of the protein. This well known technique was used to facilitate the purification of protein via metal affinity chromatography.

EXAMPLE 3

[0035] The expression vectors resulting from the preceding examples were used to express the relevant proteins. E. coli strains BL21(DE3) or BL21SI were used under inducing conditions, including 1 mM IPTG, or 300 mM NaCl, respectively, using standard methods. Proteins were then analyzed on 10-20% SDS-PAGE gels, under denaturing conditions. Each of FIGS. 1-22 presents an SDS-PAGE pattern for the proteins.

[0036] In addition to the SDS-PAGE work, the proteins were purified, by using Ni²⁺ chelating sepharose. Either proteins were mixed with charged beads, or were applied onto columns in a balanced salt buffer (0.1M Tris/0.3 M NaCl, pH 8.0). Any impurities were washed away using the same buffer, with a low concentration of imidazole (20-60 mM). Proteins of interest were then eluted, using a buffer containing imidazole at a concentration of from 0.75 to 1.0M.

EXAMPLE 4

[0037] Once the proteins were purified, they were tested for their ability to bind to antibodies in the sera of infected subjects.

[0038] Proteins were purified on 10-15% SDS-PAGE, and then blot transferred to nitrocellulose membranes. Protein was visualized with Ponceau staining.

[0039] The proteins were then contacted with either pooled sera obtained from patients who had been diagnosed with leptospiroses, or with rats immunized with Leptospira interrogans serovar Copenhageni. In the case of rats, dilutions varied from 1/500 to 1/1000. For patients, dilutions ranged from 1/100 to 1/1000. As controls, sera from healthy individuals and non-immunized rats were used.

[0040] After contact with the sera, a second antibody, either anti-rat or anti-human IgG, labeled with peroxidase was added, followed by O-phenyl diamine benzidine and hydrogen peroxide.

[0041] The results, shown in FIGS. 1-22, inclusive, show that all of the proteins reacted with sera from both sources.

[0042] In the discussion of the proteins which follows, signal and transmembrane regions were based upon the presence of hydrophobic amino acids, including Ile, Tyr, Val, Phe, Leu, Met and Ala, and Nielsen, et al., Protein Engineering 12:3-9 (1999), incorporated by reference. Each description is followed by reference to where the sequence appeared in the provisional application.

[0043] SEQ ID NO: 1 sets forth a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 2 with a predicted molecular weight of 52.7 KDa. It is a new Leptospiral lipoprotein, LpL53, according to the rules described in Haake, Microbiology 146:1491-1504 (2000), incorporated by reference. It has a hydrophobic region of a signal peptide from amino acid 4 to 10 characterized by the presence of Tyr, Leu, Ile, Phe, Leu, Phe, Ile, the lipoprotein signal peptidase cleavage site from amino acid 11-14, with Leu, Phe, Ser, Asn, and the cysteine to be lipidated at position 15 of the polypeptide sequence. (3909 & 3910)

[0044] SEQ ID NO: 3 sets forth a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 4 with a predicted molecular weight of 55 KDa. It has a signal peptide cleavage site from amino acid 1 to 28. (3531 & 3532)

[0045] SEQ ID NO: 5 sets forth a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 6 with a predicted molecular weight of 15.8 KDa. It has a signal peptide cleavage site from amino acid 1 to 38. (3489 & 3490)

[0046] SEQ ID NO: 7 sets forth a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 8 with a predicted molecular weight of 30.9 KDa. It has a signal peptide cleavage site from amino acid 1 to 19. (3871 & 3872)

[0047] SEQ ID NO: 9 sets forth a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 10 with a predicted molecular weight of 15 KDa. No match with an y deposited protein in gene bank was found with this amino acid sequence. It has a signal peptide cleavage site from amino acid 1 to 19 and a transmembrane segment from amino acid 7 to 29, partially overlapping the signal peptide sequence. (3973 & 3974)

[0048] SEQ ID NO: 11 is a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 12 with a predicted molecular weight of 20.1 KDa. It has a signal peptide cleavage site from amino acid 1 to 20. (3679 & 3680)

[0049] SEQ ID NO: 13 corresponds to a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 14 with a predicted molecular weight of 23 KDa. This polypeptide sequence is a newly identified Leptospiral lipoprotein, according to Haake, supra. It has a signal peptide hydrophobic region from amino acid 6 to 15 (Ile, Val, Tyr, Val, Ile, Tyr, Leu, Phe, Leu, Ile), characterized by a higher proportion of hydrophobic amino acids, a lipoprotein signal peptides from amino acid 16 to 19 (Ser, Leu, Tyr, Gly) and a cysteine to be lipidated at position 20 of the polypeptide sequence. (81 & 82)

[0050] SEQ ID NO: 15 sets forth a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 16 with a predicted molecular weight of 40.6 KDa. This polypeptide sequence is a newly isolated Leptospiral lipoprotein, according to the rules described in Haake, supra. It has a signal peptide hydrophobic region from amino acid 7 to 16 (Ile, Leu, Phe, Val, Leu, Thr, Gly, Phe, Ile, Phe), characterized by a higher proportion of hydrophobic amino acids, a lipoprotein signal peptides from amino acid 1 to 20 (Phe, Val, Ser, Ala) and a cysteine to be lipidated at position 21 of the polypeptide sequence. (43 & 44)

[0051] SEQ ID NO: 17 corresponds to a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 18 with a predicted molecular weight of 22.6 KDa. This polypeptide sequence is a new Leptospiral lipoprotein, according to Haake, supra. It has a signal peptide hydrophobic region from amino acid 8 to 18 (Ile, Asn, Ile, Leu, Phe, Phe, Phe, Leu, Val, Tyr, Phe), a lipoprotein signal peptidase from amino acid 19 to 22 (Leu, Leu, Phe, Gly) that conforms to the rules described in Haake and a cysteine to be lipidated at position 23 of the polypeptide sequence. (125 & 126)

[0052] SEQ ID NO: 19 corresponds to a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 20 with a predicted molecular weight of 17.3 KDa. It has a signal peptide cleavage site from amino acid 1 to 20. (3991 & 3992)

[0053] SEQ ID NO: 21 sets forth a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 22 with a predicted molecular weight of 30.9 KDa. It has a signal peptide cleavage site from amino acid 1 to 27. (3521 & 3522)

[0054] SEQ ID NO: 23 sets forth a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 24 with a predicted molecular weight of 27.1 KDa. It has a signal peptide cleavage site from amino acid 1 to 20. It has some similarity to proteins belonging to cytochrome c family. Examples are: di-haem cytochrome c peroxidase and cytochrome c, class I found in bacteria, such as Bacillus subtilis. (3533 & 3534)

[0055] SEQ ID NO: 25 corresponds to a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 26 with a predicted molecular weight of 20.9 KDa. It has a signal peptide cleavage site from amino acid 1 to 20. (3561 & 3562)

[0056] SEQ ID NO: 27 corresponds to a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 28 with a predicted molecular weight of 21.2 KDa. It has a signal peptide cleavage site from amino acid 1 to 34. It has some similarity to prokaryotic N-terminal methylation site found in bacterial general secretion pathway protein G and bacterial type II secretion system protein I/J. Examples of bacteria are E. coli, Xanthomonas campestris and Pseudomonas aeruginosa. (3675 & 3676)

[0057] SEQ ID NO: 29 corresponds to a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 30 with a predicted molecular weight of 16.6 KDa. It has a signal peptide cleavage site from amino acid 1 to 36. (3819 & 3820)

[0058] SEQ ID NO: 31 corresponds to a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 32 with a predicted molecular weight of 20.5 KDa. It has a signal peptide cleavage site from amino acid 1 to 22. (3829 & 3830)

[0059] SEQ ID NO: 33 is a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 34 with a predicted molecular weight of 20.9 KDa. It has a signal peptide cleavage site from amino acid 1 to 22. This polypeptide has some similarity to proteins having an outer membrane domain (from amino acid 77 to 182) that belong to the OmpA family. Most of these bacterial outer membrane proteins in this group are porin-like, integral membrane proteins, but some are small peptidoglycan-associated lipoprotein (such as pal). Escherichia coli is an example of a bacterium expressing a protein and having this domain. (3793 & 3794)

[0060] SEQ ID NO: 35 is a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 36 with a predicted molecular weight of 63.5 KDa. It has a signal peptide cleavage site from amino acid 1 to 29. This polypeptide has some similarity to outer membrane efflux protein identified in other bacteria. Examples include the E. coli TolC outer membrane protein; the Rhizobium nodulation protein; and the Pseudomonas FusA protein. (4007 & 4008)

[0061] SEQ ID NO: 37 is a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 38 with a predicted molecular weight of 14 KDa. It has a signal peptide cleavage site from amino acid 1 to 23. (3883 & 3884)

[0062] SEQ ID NO: 39 is a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 40 with a predicted molecular weight of 35.6 KDa. It has a signal peptide cleavage site from amino acid 1 to 36. This polypeptide sequence has some similarity to bacterial lipoproteins family identified in bacteria, such as, Escherichia coli. (2019 & 2020)

[0063] SEQ ID NO: 41 is a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 42 with a predicted molecular weight of 39.8 KDa. This protein has a transmembrane region from amino acid 68 to 90. This sequence has similarity to DshA protein of Leptospira with unknown function. (1031 & 1032)

[0064] SEQ ID NO: 43 is a polynucleotide sequence encoding an amino acid sequence as set forth in SEQ ID NO: 44 with a predicted molecular weight of 40 KDa. It is a cytoplasmic membrane protein, with one transmembrane segment from amino acid 63 to 79. This polypeptide sequence has some homology to the MoxR protein identified in Borrelia burgdorferi. The protein family (St. Louis Pfam Web site) (http://pfam.wustl.edu/) predicted two domains in this protein: (i) ATPase family domain associated with various cellular activities (AAA), such as chaperone-like functions that assist in the assembly, operation, or disassembly of protein complexes. (2517 & 2518)

[0065] SEQ ID NO: 45 corresponds to a polynucleotide segment encoding an amino acid sequence as set forth in SEQ ID NO: 46 with a predicted molecular weight of 21 KDa. This protein has a signal peptide cleavage site from amino acid 1 to 40 and a transmembrane domain from amino acid 20 to 40. The polypeptide sequence has some similarity to bacterial signal peptidases identified in bacteria, such as, Sinorhizobium meliloti and Bacillus subtilis. This is a Leptospiral membrane protein MPL21. (1991 & 1992)

[0066] The foregoing disclosure set forth various aspects of the invention, including the isolated, Leptospira surface proteins, the amino acid sequences of which are set forth as an attachment hereto, and isolated nucleic acid molecules which encode these proteins such as those set forth herein. It will be understood that once an amino acid sequence is known, various degenerate nucleotide sequences can be provided which encode that sequence. All of those are encompassed by this invention.

[0067] “Surface protein” as used herein, refers to proteins which are associated and/or exposed to the surface of the organism.

[0068] The proteins of the invention may be used, alone or in combination with each other, as or as components of vaccines. Further, they can be used as immunogens, so as to generate an antibody response. The antibodies thus generated can be used, e.g., as diagnostic tools to determine Leptospira infection or presence, as well as components of vaccines used to generate passive immunity. Proteins and antibodies may be administered “neat” or “compounded” with other standard materials used in preparing vaccines, such as carriers, adjuvants, and other materials. Intravenous formulations are one embodiment and, it will be understood that other formulations of vaccines are possible, including intradermal, subcutaneous, oral, such as sublingual forms, and others. The vaccines may be in liquid or “dry” form, such as in lyophilized form. This type of vaccine is especially suitable when it must be carried “in the field,” and used at some point in time later than when carried.

[0069] The nucleic acid molecules of the invention, as will be understood by the skilled artisan, can be used to produce the proteins described supra, via any of the recombinant methodologies well known to the skilled artisan. They can be placed in, e.g., expression vectors, under control of a promoter or other regulatory element, or they can be used “as is” to transfect or to transform cells. Eukaryotic cells, such as yeast cells, CHO cells, fibroblasts, insect cells, etc., are among the eukaryotes which can be transformed or transfected. Prokaryotes, such as E. coli or other bacteria can also be used. The choice of host cell will depend upon many factors, including whether or not glycosylation is desired, and to what end the transformant or transfectant will be used. One way these recombinant cells can be used is as in the form of a cell based vaccine, such as a whole cell vaccine. As the recombinant proteins of the invention are all surface proteins, it is to be expected that they will be expressed on the surface of host cells. If the cells are then processed so as to become non-proliferative, the cells present an ideal vaccine, especially if the host cell is one that is not normally the target of immune surveillance in the host.

[0070] Another aspect of the invention is the use of membrane preparations, or cellular “ghosts” of transformants or tranfectants. Such approaches have been used with other bacterial species, so preparation of these is well known. Transformants or transfectants which express the surface proteins of the invention can be used to prepare these materials in a fashion taught by the art.

[0071] The proteins have been discussed as vaccines, supra. It is to be understood that the vaccines of the invention can be formulated for any subject. Human vaccines are, of course, included, but so are vaccines for livestock animals, such as sheep, bovine animals, goats, pigs and so forth, and domesticated animals such as pets, confined zoo animals, etcetera. The vaccines may be used prophylactically, e.g., by administering them prior to possible exposure to Leptospira, and may also be used post exposure, in order to treat a pre-existing infection.

[0072] As will be recognized by the skilled artisan, the use of the proteins of the invention, or portions thereof, constitutes vaccination, and the protein or portion of the protein constitutes the vaccine. Upon administration to the individual or subject, in any of the ways described supra, an immune response results which protects the individual or subject when confronted with the pathogen. Such an approach, i.e., the immunization with one or more proteins or portions of proteins, can be used therapeutically or prophylactically. Passive immunization, as described supra, can also be used. In such a case, antibodies are developed against the proteins or protein portions, and via passive transfer serve a role in, e.g., prophylaxis.

[0073] It is to be understood that, while immunization with the proteins or portions of proteins can serve to stimulate an antibody response, cellular immune responses are also a part of the response of the subject to the immunization. It is well within the skill of the artisan to determine which proteins or portions of proteins function as antibody or cellular immune vaccine agents and that artisan can then formulate, e.g., “cocktails” of appropriate mixes of proteins which have the desired, immune effect.

[0074] In addition to the use of the proteins as vaccines, it is to be understood that the nucleic acid molecules described herein can also be used as vaccines. Via targeted delivery of nucleic acid molecules, one can assure an “in vivo” supply of the desired protein or protein portion molecules at a site of relevance. The artisan of delivery systems, such as liposomes, adenoviruses, retroviruses, and other formats for the delivery of DNA as immunoprophylactic or a therapeutic agents, and all are envisioned as methods for administering the vaccine. It should be kept in mind that the nucleic acid molecules of the invention include those which encode the proteins of the invention, but differ in nucleotide sequence due to codon degeneracy. Indeed, due to patterns of codon usage, which vary from organism to organism, it may be desirable to alter the sequence to maximize expression of the desired vaccine in the treated subject.

[0075] To prepare a vaccine the purified polypeptide can be isolated, lyophilized and/or stabilized, as described supra. The protein may then be adjusted to an appropriate concentration, optionally combined with a suitable vaccine adjuvant, and packaged for use. Suitable adjuvants include but are not limited to: surfactants and pluronic polyols; polyanions, e.g., pyran, dextran sulfate, poly IC; polyacrylics, carbopol; peptides, e.g., muramyl dipeptide, dimethylglycine, oil emulsions, vitamins, cytokines, hormones, aluminum, calcium salts, and mixtures thereof, bacterial and plant products, e.g., Bacillus Calmette-Guerin (BCG), complete Freund's adjuvant, and threalose. Alternatively, the immunogenic protein may be incorporated into liposomes for use in a vaccine formulation, may be fused to other immunogenic proteins, or may be conjugated to polysaccharides or other polymers. See Edelman, in New Generation Vaccines (Marshall Decker, N.Y. 1997), incorporated by reference.

[0076] The weight of the immunogenic protein included in a given dosage of vaccine can vary widely, e.g., from 5 ug-300 mg., and depends on: the age, weight, and physical condition of the animal or the human subject considered for vaccination.

[0077] In addition, the nucleic acid molecules of the invention can be used as vaccines. The rational of this approach is that the DNA will produce the protein following injection thus in turn inducing the desired immune response.

[0078] For such vaccines, a pharmaceutical composition can include either a mammalian recombinant expression vector, such as pTARGET, or a construct such as an expression vector, which includes a nucleic acid molecule encoding the protein, operatively linked to transcription control/terminator sequences, combined with a pharmaceutically acceptable carrier. These may include, but are not limited to, aqueous physiologically balanced solutions, artificial lipid-containing substrates, natural lipid-containing substrates, oils, esters, and glycols. Pharmaceutically acceptable carriers can also include a suitable delivery vehicle, such as liposomes, micelles, and cells. Adjuvants for DNA based vaccines can be used, such as CpG oligonucleotides and cytonkines. The vaccines can also be delivered by attenuated bacteria, such as Salmonella.

[0079] Another feature of the invention is the use of the proteins, or portions of the proteins of the invention, as well as nucleic acid molecules and portions of nucleic acid molecules, in the manufacture of kits useful for diagnosis of Leptospira infection, either “in the field” or in the laboratory. Such kits involve, e.g., the protein, protein portion, nucleic acid molecule, or nucleic acid molecule portion, in combination with, e.g., a solid phase, such as a bead, mutltiwell plate, etc., to which the component is affixed. The kit can then be used by contacting a sample of interest thereto, followed by a second component, which can also be included in the kit, such as a labeled protein or proteins portion, or labeled nucleic acid molecule or portion of a nucleic acid molecule. When nucleic acid molecules are used in the diagnostic kits of the invention, it is desirable that each portion hybridize to a separate portion of a target nucleic acid molecule.

[0080] It may be desirable to screen the proteins and nucleic acid molecules of the invention in, e.g., and animal or cellular model prior to administration to large animals or humans. Standard practice tests a potential vaccine in, e.g., a hamster, mouse, rat or other rodent model to determine it efficacy and strength, and the molecules of this invention may be so tested as well. Testing of the DNA molecules in, e.g., microorganisms such as E. coli or other prokaryotes or eukaryote organisms can be carried out to deter mine which are, in fact, good producers, i.e., molecules which produce high yields, and/or produce transformants which react well to culture. Other aspects of the inventions will be clear to the skilled artisan, and need not be reiterated here.

1 46 1 1431 DNA Leptospira interrogans serovar copenhageni CDS (1)...(1428) 1 ttg gtt cgt tat tta att ttt ctt ttt att tta ttt tcg aat tgt tta 48 Leu Val Arg Tyr Leu Ile Phe Leu Phe Ile Leu Phe Ser Asn Cys Leu 1 5 10 15 cct acc aat gtg ttt ggt ata gcg gcc ccc gaa aac att gat tat tgg 96 Pro Thr Asn Val Phe Gly Ile Ala Ala Pro Glu Asn Ile Asp Tyr Trp 20 25 30 att cat ttt cta ctg aaa att ccg gat ttt ctt tta cag aat aac gat 144 Ile His Phe Leu Leu Lys Ile Pro Asp Phe Leu Leu Gln Asn Asn Asp 35 40 45 cca ctt cac tca gat tct caa tct gac tca aga tta gat tgg acc tta 192 Pro Leu His Ser Asp Ser Gln Ser Asp Ser Arg Leu Asp Trp Thr Leu 50 55 60 tta atc gga gct gaa aat gct caa acg gca agt aaa ggt atc tac gta 240 Leu Ile Gly Ala Glu Asn Ala Gln Thr Ala Ser Lys Gly Ile Tyr Val 65 70 75 80 gat caa aat ggt ttt atc tac gta gtt ggt gaa acc aat gga ggt gtt 288 Asp Gln Asn Gly Phe Ile Tyr Val Val Gly Glu Thr Asn Gly Gly Val 85 90 95 tat aat ccg aga cca atc gga atg aaa gat ctc att tta gga aag tat 336 Tyr Asn Pro Arg Pro Ile Gly Met Lys Asp Leu Ile Leu Gly Lys Tyr 100 105 110 gat tct cat aaa aat aca atc tgg act caa caa att gga gct att gac 384 Asp Ser His Lys Asn Thr Ile Trp Thr Gln Gln Ile Gly Ala Ile Asp 115 120 125 gta gca ttg aat gtt agc gct atg act gtc gat cat aac gga aat gtt 432 Val Ala Leu Asn Val Ser Ala Met Thr Val Asp His Asn Gly Asn Val 130 135 140 tac gtt acc ggt agt acg ggc aat gat gga ttt ttt ccc aac cca ctt 480 Tyr Val Thr Gly Ser Thr Gly Asn Asp Gly Phe Phe Pro Asn Pro Leu 145 150 155 160 cgt agt tca gaa gat atg ttc gta att aaa ttc aac tcg gac gga acc 528 Arg Ser Ser Glu Asp Met Phe Val Ile Lys Phe Asn Ser Asp Gly Thr 165 170 175 aga gat tgg act aca caa gcc ggc cca cag gaa aaa gaa tcc aga aca 576 Arg Asp Trp Thr Thr Gln Ala Gly Pro Gln Glu Lys Glu Ser Arg Thr 180 185 190 act cca aca agt att tat ata gat aca tct gga aat att ttt gta gtt 624 Thr Pro Thr Ser Ile Tyr Ile Asp Thr Ser Gly Asn Ile Phe Val Val 195 200 205 ggg ttt tca agc gga cct ttc gga ggt ccg gaa tta ggg gcg aac gga 672 Gly Phe Ser Ser Gly Pro Phe Gly Gly Pro Glu Leu Gly Ala Asn Gly 210 215 220 ttt ata gct aaa ttt gat cct caa gga aat caa act tgg gtc aga caa 720 Phe Ile Ala Lys Phe Asp Pro Gln Gly Asn Gln Thr Trp Val Arg Gln 225 230 235 240 ctt ttc att agt aga cat act caa atc tcc aca cta tgt gcc gct ttc 768 Leu Phe Ile Ser Arg His Thr Gln Ile Ser Thr Leu Cys Ala Ala Phe 245 250 255 gac aga gtt caa aat act tat gta acc ggt tcg gga aac gca aat ttt 816 Asp Arg Val Gln Asn Thr Tyr Val Thr Gly Ser Gly Asn Ala Asn Phe 260 265 270 gaa acg aat aca gag ata aat gac ttc ggc gtg aaa aat ctt ttt att 864 Glu Thr Asn Thr Glu Ile Asn Asp Phe Gly Val Lys Asn Leu Phe Ile 275 280 285 ttc aaa tat gat aac gat aat gga aac aaa caa ttt ttc gct caa ctt 912 Phe Lys Tyr Asp Asn Asp Asn Gly Asn Lys Gln Phe Phe Ala Gln Leu 290 295 300 agt ttc cct tca aga tca att gaa agt aat act ata aca gtt gat act 960 Ser Phe Pro Ser Arg Ser Ile Glu Ser Asn Thr Ile Thr Val Asp Thr 305 310 315 320 tta gga aac gtt ttt gta ggt gga aat agc aac gct gat ttt gga tcc 1008 Leu Gly Asn Val Phe Val Gly Gly Asn Ser Asn Ala Asp Phe Gly Ser 325 330 335 ggt gct gac aga acg tct cat ctt gca acc ttg gta aaa tac aat tct 1056 Gly Ala Asp Arg Thr Ser His Leu Ala Thr Leu Val Lys Tyr Asn Ser 340 345 350 tta ggt gtt ctt caa tgg atc caa caa tta ggc ccg gca caa agc caa 1104 Leu Gly Val Leu Gln Trp Ile Gln Gln Leu Gly Pro Ala Gln Ser Gln 355 360 365 gat cct caa aat aat tat cat act act att tct tct cta gat aca gat 1152 Asp Pro Gln Asn Asn Tyr His Thr Thr Ile Ser Ser Leu Asp Thr Asp 370 375 380 act gag gga aat gtc tat tca ata ggt tct aca aat gga aat ata tta 1200 Thr Glu Gly Asn Val Tyr Ser Ile Gly Ser Thr Asn Gly Asn Ile Leu 385 390 395 400 aaa gta cat gaa aac tct acc ggt att cga gat cta ttt ttt aca aaa 1248 Lys Val His Glu Asn Ser Thr Gly Ile Arg Asp Leu Phe Phe Thr Lys 405 410 415 cac aat cct tcc gga gaa tta atc tgg tca cga caa ata ggc gct cct 1296 His Asn Pro Ser Gly Glu Leu Ile Trp Ser Arg Gln Ile Gly Ala Pro 420 425 430 aat aga ctt aaa att ggt aat gga ata gca cat gac tta aat gga aat 1344 Asn Arg Leu Lys Ile Gly Asn Gly Ile Ala His Asp Leu Asn Gly Asn 435 440 445 tta tat tac atg ggg aat aca aac gaa tat cta cat gaa gaa gcc gct 1392 Leu Tyr Tyr Met Gly Asn Thr Asn Glu Tyr Leu His Glu Glu Ala Ala 450 455 460 gtg cat gac tta tat ata ttc atc gtc aaa tat aaa tga 1431 Val His Asp Leu Tyr Ile Phe Ile Val Lys Tyr Lys 465 470 475 2 476 PRT Leptospira interrogans serovar copenhageni 2 Leu Val Arg Tyr Leu Ile Phe Leu Phe Ile Leu Phe Ser Asn Cys Leu 1 5 10 15 Pro Thr Asn Val Phe Gly Ile Ala Ala Pro Glu Asn Ile Asp Tyr Trp 20 25 30 Ile His Phe Leu Leu Lys Ile Pro Asp Phe Leu Leu Gln Asn Asn Asp 35 40 45 Pro Leu His Ser Asp Ser Gln Ser Asp Ser Arg Leu Asp Trp Thr Leu 50 55 60 Leu Ile Gly Ala Glu Asn Ala Gln Thr Ala Ser Lys Gly Ile Tyr Val 65 70 75 80 Asp Gln Asn Gly Phe Ile Tyr Val Val Gly Glu Thr Asn Gly Gly Val 85 90 95 Tyr Asn Pro Arg Pro Ile Gly Met Lys Asp Leu Ile Leu Gly Lys Tyr 100 105 110 Asp Ser His Lys Asn Thr Ile Trp Thr Gln Gln Ile Gly Ala Ile Asp 115 120 125 Val Ala Leu Asn Val Ser Ala Met Thr Val Asp His Asn Gly Asn Val 130 135 140 Tyr Val Thr Gly Ser Thr Gly Asn Asp Gly Phe Phe Pro Asn Pro Leu 145 150 155 160 Arg Ser Ser Glu Asp Met Phe Val Ile Lys Phe Asn Ser Asp Gly Thr 165 170 175 Arg Asp Trp Thr Thr Gln Ala Gly Pro Gln Glu Lys Glu Ser Arg Thr 180 185 190 Thr Pro Thr Ser Ile Tyr Ile Asp Thr Ser Gly Asn Ile Phe Val Val 195 200 205 Gly Phe Ser Ser Gly Pro Phe Gly Gly Pro Glu Leu Gly Ala Asn Gly 210 215 220 Phe Ile Ala Lys Phe Asp Pro Gln Gly Asn Gln Thr Trp Val Arg Gln 225 230 235 240 Leu Phe Ile Ser Arg His Thr Gln Ile Ser Thr Leu Cys Ala Ala Phe 245 250 255 Asp Arg Val Gln Asn Thr Tyr Val Thr Gly Ser Gly Asn Ala Asn Phe 260 265 270 Glu Thr Asn Thr Glu Ile Asn Asp Phe Gly Val Lys Asn Leu Phe Ile 275 280 285 Phe Lys Tyr Asp Asn Asp Asn Gly Asn Lys Gln Phe Phe Ala Gln Leu 290 295 300 Ser Phe Pro Ser Arg Ser Ile Glu Ser Asn Thr Ile Thr Val Asp Thr 305 310 315 320 Leu Gly Asn Val Phe Val Gly Gly Asn Ser Asn Ala Asp Phe Gly Ser 325 330 335 Gly Ala Asp Arg Thr Ser His Leu Ala Thr Leu Val Lys Tyr Asn Ser 340 345 350 Leu Gly Val Leu Gln Trp Ile Gln Gln Leu Gly Pro Ala Gln Ser Gln 355 360 365 Asp Pro Gln Asn Asn Tyr His Thr Thr Ile Ser Ser Leu Asp Thr Asp 370 375 380 Thr Glu Gly Asn Val Tyr Ser Ile Gly Ser Thr Asn Gly Asn Ile Leu 385 390 395 400 Lys Val His Glu Asn Ser Thr Gly Ile Arg Asp Leu Phe Phe Thr Lys 405 410 415 His Asn Pro Ser Gly Glu Leu Ile Trp Ser Arg Gln Ile Gly Ala Pro 420 425 430 Asn Arg Leu Lys Ile Gly Asn Gly Ile Ala His Asp Leu Asn Gly Asn 435 440 445 Leu Tyr Tyr Met Gly Asn Thr Asn Glu Tyr Leu His Glu Glu Ala Ala 450 455 460 Val His Asp Leu Tyr Ile Phe Ile Val Lys Tyr Lys 465 470 475 3 1470 DNA Leptospira interrogans serovar copenhageni CDS (1)...(1467) 3 ttg ttc gag gga aac atg aga ata ttt caa att tat ata att cta ttg 48 Leu Phe Glu Gly Asn Met Arg Ile Phe Gln Ile Tyr Ile Ile Leu Leu 1 5 10 15 ttg tcc tta ttc ctg gcc cga acg gca tat tcg gaa caa atc gta tcc 96 Leu Ser Leu Phe Leu Ala Arg Thr Ala Tyr Ser Glu Gln Ile Val Ser 20 25 30 tca aaa aaa gac gaa ccg gat gct tac tac gga ctg gat gta aaa gcg 144 Ser Lys Lys Asp Glu Pro Asp Ala Tyr Tyr Gly Leu Asp Val Lys Ala 35 40 45 gtc att tcc cct tcc tac gga gcc aga att aga gac ggc gca tct ggt 192 Val Ile Ser Pro Ser Tyr Gly Ala Arg Ile Arg Asp Gly Ala Ser Gly 50 55 60 att tcc aac tcg gct cca aat gat aag aca ggg ttt tcc act cct tgg 240 Ile Ser Asn Ser Ala Pro Asn Asp Lys Thr Gly Phe Ser Thr Pro Trp 65 70 75 80 acc att ctt atg att tct aaa acg ttt gaa gaa acc gga atc caa gca 288 Thr Ile Leu Met Ile Ser Lys Thr Phe Glu Glu Thr Gly Ile Gln Ala 85 90 95 gaa ctc tgg ggg gaa ctt atc aga aac aac caa cta aca tcg gat aca 336 Glu Leu Trp Gly Glu Leu Ile Arg Asn Asn Gln Leu Thr Ser Asp Thr 100 105 110 cga act gac tct gga aca aaa caa aat cct tat att cta aac gtt cgt 384 Arg Thr Asp Ser Gly Thr Lys Gln Asn Pro Tyr Ile Leu Asn Val Arg 115 120 125 aga gcc agt att aaa aag aat tgg gaa act tct tcc tat ggc aat tat 432 Arg Ala Ser Ile Lys Lys Asn Trp Glu Thr Ser Ser Tyr Gly Asn Tyr 130 135 140 tct atc ggt ttc gga att caa gaa tta cct cat aca tac act cag tgg 480 Ser Ile Gly Phe Gly Ile Gln Glu Leu Pro His Thr Tyr Thr Gln Trp 145 150 155 160 agt aac tat tgg aga tgg aga tat att gac aaa ggt cct tta gaa tct 528 Ser Asn Tyr Trp Arg Trp Arg Tyr Ile Asp Lys Gly Pro Leu Glu Ser 165 170 175 ctt ggt ttt gca cct caa ccc gcc gac ata gga ttg aat gcg acc gga 576 Leu Gly Phe Ala Pro Gln Pro Ala Asp Ile Gly Leu Asn Ala Thr Gly 180 185 190 aaa tgg tcc att ttc agc gca caa att atg atc agt aac gga gaa ggt 624 Lys Trp Ser Ile Phe Ser Ala Gln Ile Met Ile Ser Asn Gly Glu Gly 195 200 205 tat aga gaa acc caa aac aca aat tct tcc gga atg gac gtt tcc tcc 672 Tyr Arg Glu Thr Gln Asn Thr Asn Ser Ser Gly Met Asp Val Ser Ser 210 215 220 aga ttt tcc att gaa cct atg tta ggc gaa aaa acc aaa acg ggg ctt 720 Arg Phe Ser Ile Glu Pro Met Leu Gly Glu Lys Thr Lys Thr Gly Leu 225 230 235 240 cat tta ttt tat aga aaa gaa aac gct ttc ggc ttt gga gga aac gaa 768 His Leu Phe Tyr Arg Lys Glu Asn Ala Phe Gly Phe Gly Gly Asn Glu 245 250 255 tgt ttc gaa ggg aaa aca aac tgt ctt cca aac gat cta aat ccg gct 816 Cys Phe Glu Gly Lys Thr Asn Cys Leu Pro Asn Asp Leu Asn Pro Ala 260 265 270 act tca tta tat aga caa att caa agt tta cag tcc gac act ttt ggt 864 Thr Ser Leu Tyr Arg Gln Ile Gln Ser Leu Gln Ser Asp Thr Phe Gly 275 280 285 tca gaa tcc aat ttg att tgg aat ggt ttt ttg act tgg aat cta ggt 912 Ser Glu Ser Asn Leu Ile Trp Asn Gly Phe Leu Thr Trp Asn Leu Gly 290 295 300 ttg ggc gga att ctc aaa aaa caa aac agc gga gaa atc cga gat aga 960 Leu Gly Gly Ile Leu Lys Lys Gln Asn Ser Gly Glu Ile Arg Asp Arg 305 310 315 320 ctt cag ccg ttt gca cct ccg att gct ttc gga aaa gac ggt ttc gga 1008 Leu Gln Pro Phe Ala Pro Pro Ile Ala Phe Gly Lys Asp Gly Phe Gly 325 330 335 aag gcg tta tac att tgg tta tcc ata ggc atc gaa aaa ttt cat ctt 1056 Lys Ala Leu Tyr Ile Trp Leu Ser Ile Gly Ile Glu Lys Phe His Leu 340 345 350 ctg ggg aga ata gaa caa ggc aca gga aac aac gga att atg ggt gtc 1104 Leu Gly Arg Ile Glu Gln Gly Thr Gly Asn Asn Gly Ile Met Gly Val 355 360 365 acc gac acg gta caa aaa gaa ttt cta cct ggt tta gga att cca aat 1152 Thr Asp Thr Val Gln Lys Glu Phe Leu Pro Gly Leu Gly Ile Pro Asn 370 375 380 gta gat gct aca tta caa att cgg aat att ctc cca gaa acc aga gca 1200 Val Asp Ala Thr Leu Gln Ile Arg Asn Ile Leu Pro Glu Thr Arg Ala 385 390 395 400 ggt gga tat tcc agt aaa agt tca ttt aga agg atc agt gtg ttt ttc 1248 Gly Gly Tyr Ser Ser Lys Ser Ser Phe Arg Arg Ile Ser Val Phe Phe 405 410 415 gaa tgg att gta aat ccc aga ttt aga atg gca atc ggc tat atc gaa 1296 Glu Trp Ile Val Asn Pro Arg Phe Arg Met Ala Ile Gly Tyr Ile Glu 420 425 430 aat aaa aat tat gat ttg aac gga ata tcc caa cgc gct tat atc gat 1344 Asn Lys Asn Tyr Asp Leu Asn Gly Ile Ser Gln Arg Ala Tyr Ile Asp 435 440 445 cca ctc ggg aat gaa aga act gaa aaa gaa tat ctt tct caa tgg aaa 1392 Pro Leu Gly Asn Glu Arg Thr Glu Lys Glu Tyr Leu Ser Gln Trp Lys 450 455 460 gag tca gga aac tta gga att gtt tct tat tcg gtt ttg gat aaa caa 1440 Glu Ser Gly Asn Leu Gly Ile Val Ser Tyr Ser Val Leu Asp Lys Gln 465 470 475 480 ata ctt tta aga act aca ata gaa ttc taa 1470 Ile Leu Leu Arg Thr Thr Ile Glu Phe 485 4 489 PRT Leptospira interrogans serovar copenhageni 4 Leu Phe Glu Gly Asn Met Arg Ile Phe Gln Ile Tyr Ile Ile Leu Leu 1 5 10 15 Leu Ser Leu Phe Leu Ala Arg Thr Ala Tyr Ser Glu Gln Ile Val Ser 20 25 30 Ser Lys Lys Asp Glu Pro Asp Ala Tyr Tyr Gly Leu Asp Val Lys Ala 35 40 45 Val Ile Ser Pro Ser Tyr Gly Ala Arg Ile Arg Asp Gly Ala Ser Gly 50 55 60 Ile Ser Asn Ser Ala Pro Asn Asp Lys Thr Gly Phe Ser Thr Pro Trp 65 70 75 80 Thr Ile Leu Met Ile Ser Lys Thr Phe Glu Glu Thr Gly Ile Gln Ala 85 90 95 Glu Leu Trp Gly Glu Leu Ile Arg Asn Asn Gln Leu Thr Ser Asp Thr 100 105 110 Arg Thr Asp Ser Gly Thr Lys Gln Asn Pro Tyr Ile Leu Asn Val Arg 115 120 125 Arg Ala Ser Ile Lys Lys Asn Trp Glu Thr Ser Ser Tyr Gly Asn Tyr 130 135 140 Ser Ile Gly Phe Gly Ile Gln Glu Leu Pro His Thr Tyr Thr Gln Trp 145 150 155 160 Ser Asn Tyr Trp Arg Trp Arg Tyr Ile Asp Lys Gly Pro Leu Glu Ser 165 170 175 Leu Gly Phe Ala Pro Gln Pro Ala Asp Ile Gly Leu Asn Ala Thr Gly 180 185 190 Lys Trp Ser Ile Phe Ser Ala Gln Ile Met Ile Ser Asn Gly Glu Gly 195 200 205 Tyr Arg Glu Thr Gln Asn Thr Asn Ser Ser Gly Met Asp Val Ser Ser 210 215 220 Arg Phe Ser Ile Glu Pro Met Leu Gly Glu Lys Thr Lys Thr Gly Leu 225 230 235 240 His Leu Phe Tyr Arg Lys Glu Asn Ala Phe Gly Phe Gly Gly Asn Glu 245 250 255 Cys Phe Glu Gly Lys Thr Asn Cys Leu Pro Asn Asp Leu Asn Pro Ala 260 265 270 Thr Ser Leu Tyr Arg Gln Ile Gln Ser Leu Gln Ser Asp Thr Phe Gly 275 280 285 Ser Glu Ser Asn Leu Ile Trp Asn Gly Phe Leu Thr Trp Asn Leu Gly 290 295 300 Leu Gly Gly Ile Leu Lys Lys Gln Asn Ser Gly Glu Ile Arg Asp Arg 305 310 315 320 Leu Gln Pro Phe Ala Pro Pro Ile Ala Phe Gly Lys Asp Gly Phe Gly 325 330 335 Lys Ala Leu Tyr Ile Trp Leu Ser Ile Gly Ile Glu Lys Phe His Leu 340 345 350 Leu Gly Arg Ile Glu Gln Gly Thr Gly Asn Asn Gly Ile Met Gly Val 355 360 365 Thr Asp Thr Val Gln Lys Glu Phe Leu Pro Gly Leu Gly Ile Pro Asn 370 375 380 Val Asp Ala Thr Leu Gln Ile Arg Asn Ile Leu Pro Glu Thr Arg Ala 385 390 395 400 Gly Gly Tyr Ser Ser Lys Ser Ser Phe Arg Arg Ile Ser Val Phe Phe 405 410 415 Glu Trp Ile Val Asn Pro Arg Phe Arg Met Ala Ile Gly Tyr Ile Glu 420 425 430 Asn Lys Asn Tyr Asp Leu Asn Gly Ile Ser Gln Arg Ala Tyr Ile Asp 435 440 445 Pro Leu Gly Asn Glu Arg Thr Glu Lys Glu Tyr Leu Ser Gln Trp Lys 450 455 460 Glu Ser Gly Asn Leu Gly Ile Val Ser Tyr Ser Val Leu Asp Lys Gln 465 470 475 480 Ile Leu Leu Arg Thr Thr Ile Glu Phe 485 5 420 DNA Leptospira interrogans serovar copenhageni CDS (1)...(417) 5 atg aga ttc aaa tcg aga tta ttt ttt tct tgt atg atc gtt ttt ttg 48 Met Arg Phe Lys Ser Arg Leu Phe Phe Ser Cys Met Ile Val Phe Leu 1 5 10 15 agc aca act ctg ata gca tat aca atc ctt ccg tgt tct ttt ggt tta 96 Ser Thr Thr Leu Ile Ala Tyr Thr Ile Leu Pro Cys Ser Phe Gly Leu 20 25 30 gat gct tgt tcc tgt gaa cca act cgg gga gaa acg ttg att agt tct 144 Asp Ala Cys Ser Cys Glu Pro Thr Arg Gly Glu Thr Leu Ile Ser Ser 35 40 45 ctc tta ttt tta aca act aac tct gat aaa acg tcc tgt cat agt att 192 Leu Leu Phe Leu Thr Thr Asn Ser Asp Lys Thr Ser Cys His Ser Ile 50 55 60 acg gat tct gta tgt tac gaa agt ttt cat tcc gat tcg ttt tca att 240 Thr Asp Ser Val Cys Tyr Glu Ser Phe His Ser Asp Ser Phe Ser Ile 65 70 75 80 tta tgc aaa atg tct aat gct gaa atc cgt tta aat gac gtc tgt tct 288 Leu Cys Lys Met Ser Asn Ala Glu Ile Arg Leu Asn Asp Val Cys Ser 85 90 95 gat caa aat tca gtt gga gat tgt tat cta gat aat tta cga ttg acg 336 Asp Gln Asn Ser Val Gly Asp Cys Tyr Leu Asp Asn Leu Arg Leu Thr 100 105 110 ttt tat aac gat act tat act tct aag gcc gca gaa gat tat tgt aaa 384 Phe Tyr Asn Asp Thr Tyr Thr Ser Lys Ala Ala Glu Asp Tyr Cys Lys 115 120 125 aat caa ctg aga gga ttt ttt tac aat aat aga tga 420 Asn Gln Leu Arg Gly Phe Phe Tyr Asn Asn Arg 130 135 6 139 PRT Leptospira interrogans serovar copenhageni 6 Met Arg Phe Lys Ser Arg Leu Phe Phe Ser Cys Met Ile Val Phe Leu 1 5 10 15 Ser Thr Thr Leu Ile Ala Tyr Thr Ile Leu Pro Cys Ser Phe Gly Leu 20 25 30 Asp Ala Cys Ser Cys Glu Pro Thr Arg Gly Glu Thr Leu Ile Ser Ser 35 40 45 Leu Leu Phe Leu Thr Thr Asn Ser Asp Lys Thr Ser Cys His Ser Ile 50 55 60 Thr Asp Ser Val Cys Tyr Glu Ser Phe His Ser Asp Ser Phe Ser Ile 65 70 75 80 Leu Cys Lys Met Ser Asn Ala Glu Ile Arg Leu Asn Asp Val Cys Ser 85 90 95 Asp Gln Asn Ser Val Gly Asp Cys Tyr Leu Asp Asn Leu Arg Leu Thr 100 105 110 Phe Tyr Asn Asp Thr Tyr Thr Ser Lys Ala Ala Glu Asp Tyr Cys Lys 115 120 125 Asn Gln Leu Arg Gly Phe Phe Tyr Asn Asn Arg 130 135 7 918 DNA Leptospira interrogans serovar copenhageni CDS (1)...(915) 7 gtg ttt gaa aac aat gta gga gaa aat atg att caa aaa tcg att tta 48 Val Phe Glu Asn Asn Val Gly Glu Asn Met Ile Gln Lys Ser Ile Leu 1 5 10 15 ata ttt ctg gtc ttt ctt tcc ttc gtg gtt tgt aag aag gat tcc aac 96 Ile Phe Leu Val Phe Leu Ser Phe Val Val Cys Lys Lys Asp Ser Asn 20 25 30 gat gat gat ctt act gta gct gct ttg gcc gcg ctt tct ggc gga tat 144 Asp Asp Asp Leu Thr Val Ala Ala Leu Ala Ala Leu Ser Gly Gly Tyr 35 40 45 tgt aat gga agt tca gct aat acg gga att aca gta tct aag ggt acg 192 Cys Asn Gly Ser Ser Ala Asn Thr Gly Ile Thr Val Ser Lys Gly Thr 50 55 60 gca act ttg gat gca tcc tca ggt tgt gtt acc gga gtg act act tgt 240 Ala Thr Leu Asp Ala Ser Ser Gly Cys Val Thr Gly Val Thr Thr Cys 65 70 75 80 atg gat tca gcg ctt cct act tgg atc aag aat aac ttt aaa tgt tcc 288 Met Asp Ser Ala Leu Pro Thr Trp Ile Lys Asn Asn Phe Lys Cys Ser 85 90 95 gta gct tat gta tct ggt tcc agt tat ata ttt aaa tct cag aac gtt 336 Val Ala Tyr Val Ser Gly Ser Ser Tyr Ile Phe Lys Ser Gln Asn Val 100 105 110 ccc aat acg aaa agt tat tat tac ggt tca agt tct cct ttg ttt gaa 384 Pro Asn Thr Lys Ser Tyr Tyr Tyr Gly Ser Ser Ser Pro Leu Phe Glu 115 120 125 aca ctt ccg aca gga aat atg cct gca gga aat aat tcc gtt tcg agt 432 Thr Leu Pro Thr Gly Asn Met Pro Ala Gly Asn Asn Ser Val Ser Ser 130 135 140 caa aaa ttc gtt tat acg att cct tcc agt ccc ata aaa gga agt gga 480 Gln Lys Phe Val Tyr Thr Ile Pro Ser Ser Pro Ile Lys Gly Ser Gly 145 150 155 160 act gtc gga aca caa ggc gga ctt gtg tcg ata gga att aca gta aac 528 Thr Val Gly Thr Gln Gly Gly Leu Val Ser Ile Gly Ile Thr Val Asn 165 170 175 ggt ctt gcg att ttt aat aac gca gcc aat cca cct gat act ctc gca 576 Gly Leu Ala Ile Phe Asn Asn Ala Ala Asn Pro Pro Asp Thr Leu Ala 180 185 190 gtg gag gct cag act ttt gat aac ttt gga ggc cat cct caa aat aca 624 Val Glu Ala Gln Thr Phe Asp Asn Phe Gly Gly His Pro Gln Asn Thr 195 200 205 ggg gtt tat cac cat cac gca gcg gta aca aag gtg agt aac aac gat 672 Gly Val Tyr His His His Ala Ala Val Thr Lys Val Ser Asn Asn Asp 210 215 220 tca aat ttg atc gga gtg att ttg gat ggt tac gca att tac gga aaa 720 Ser Asn Leu Ile Gly Val Ile Leu Asp Gly Tyr Ala Ile Tyr Gly Lys 225 230 235 240 aaa tgc gat aac gga act tcg tca act gga gat gac ttt gtc cca act 768 Lys Cys Asp Asn Gly Thr Ser Ser Thr Gly Asp Asp Phe Val Pro Thr 245 250 255 gat ttg gat aat ttg cat ggg cat aca aaa gct acg gtt cac ttt tct 816 Asp Leu Asp Asn Leu His Gly His Thr Lys Ala Thr Val His Phe Ser 260 265 270 act cca act tat cac tat cac ttt gct cct gat gct act gca ggg att 864 Thr Pro Thr Tyr His Tyr His Phe Ala Pro Asp Ala Thr Ala Gly Ile 275 280 285 gac act ttg atg ggt tcc ttt ttt tac gga acg ata gga agt gtt tcc 912 Asp Thr Leu Met Gly Ser Phe Phe Tyr Gly Thr Ile Gly Ser Val Ser 290 295 300 aac taa 918 Asn 305 8 305 PRT Leptospira interrogans serovar copenhageni 8 Val Phe Glu Asn Asn Val Gly Glu Asn Met Ile Gln Lys Ser Ile Leu 1 5 10 15 Ile Phe Leu Val Phe Leu Ser Phe Val Val Cys Lys Lys Asp Ser Asn 20 25 30 Asp Asp Asp Leu Thr Val Ala Ala Leu Ala Ala Leu Ser Gly Gly Tyr 35 40 45 Cys Asn Gly Ser Ser Ala Asn Thr Gly Ile Thr Val Ser Lys Gly Thr 50 55 60 Ala Thr Leu Asp Ala Ser Ser Gly Cys Val Thr Gly Val Thr Thr Cys 65 70 75 80 Met Asp Ser Ala Leu Pro Thr Trp Ile Lys Asn Asn Phe Lys Cys Ser 85 90 95 Val Ala Tyr Val Ser Gly Ser Ser Tyr Ile Phe Lys Ser Gln Asn Val 100 105 110 Pro Asn Thr Lys Ser Tyr Tyr Tyr Gly Ser Ser Ser Pro Leu Phe Glu 115 120 125 Thr Leu Pro Thr Gly Asn Met Pro Ala Gly Asn Asn Ser Val Ser Ser 130 135 140 Gln Lys Phe Val Tyr Thr Ile Pro Ser Ser Pro Ile Lys Gly Ser Gly 145 150 155 160 Thr Val Gly Thr Gln Gly Gly Leu Val Ser Ile Gly Ile Thr Val Asn 165 170 175 Gly Leu Ala Ile Phe Asn Asn Ala Ala Asn Pro Pro Asp Thr Leu Ala 180 185 190 Val Glu Ala Gln Thr Phe Asp Asn Phe Gly Gly His Pro Gln Asn Thr 195 200 205 Gly Val Tyr His His His Ala Ala Val Thr Lys Val Ser Asn Asn Asp 210 215 220 Ser Asn Leu Ile Gly Val Ile Leu Asp Gly Tyr Ala Ile Tyr Gly Lys 225 230 235 240 Lys Cys Asp Asn Gly Thr Ser Ser Thr Gly Asp Asp Phe Val Pro Thr 245 250 255 Asp Leu Asp Asn Leu His Gly His Thr Lys Ala Thr Val His Phe Ser 260 265 270 Thr Pro Thr Tyr His Tyr His Phe Ala Pro Asp Ala Thr Ala Gly Ile 275 280 285 Asp Thr Leu Met Gly Ser Phe Phe Tyr Gly Thr Ile Gly Ser Val Ser 290 295 300 Asn 305 9 399 DNA Leptospira interrogans serovar copenhageni CDS (1)...(396) 9 atg cgt ata aga tat atc aca ttt ctt att ttc atg atc cca gcc att 48 Met Arg Ile Arg Tyr Ile Thr Phe Leu Ile Phe Met Ile Pro Ala Ile 1 5 10 15 cta aca atc tcg gtt att tta gct tat ata att gta atg cgt gct gtc 48 Leu Thr Ile Ser Val Ile Leu Ala Tyr Ile Ile Val Met Arg Ala Val 20 25 30 agt aga gaa act tgt gaa aaa aat ctc cga gga ctt tgg tat ttg act 144 Ser Arg Glu Thr Cys Glu Lys Asn Leu Arg Gly Leu Trp Tyr Leu Thr 35 40 45 tct ata ggg agt cgt tgt gtt ctt gct act gaa tgt ttt tat cgt ggc 192 Ser Ile Gly Ser Arg Cys Val Leu Ala Thr Glu Cys Phe Tyr Arg Gly 50 55 60 aac tgt ttg cca tcg tac gat gca gtt act aat tgc gaa cgg ctt ttg 240 Asn Cys Leu Pro Ser Tyr Asp Ala Val Thr Asn Cys Glu Arg Leu Leu 65 70 75 80 atc ggc gaa gaa agg aaa tat gtg tat tta cag ttg gga atg cct gta 288 Ile Gly Glu Glu Arg Lys Tyr Val Tyr Leu Gln Leu Gly Met Pro Val 85 90 95 aga agt gga agt ggt cat gag tat ttt gac gga ggt gct atg aat cgt 336 Arg Ser Gly Ser Gly His Glu Tyr Phe Asp Gly Gly Ala Met Asn Arg 100 105 110 tct gaa tta tcc gtt gaa ttc aat cat aat cga tta gtt aaa aaa aat 384 Ser Glu Leu Ser Val Glu Phe Asn His Asn Arg Leu Val Lys Lys Asn 115 120 125 tgt aga ttt gaa tag 399 Cys Arg Phe Glu 130 10 132 PRT Leptospira interrogans serovar copenhageni 10 Met Arg Ile Arg Tyr Ile Thr Phe Leu Ile Phe Met Ile Pro Ala Ile 1 5 10 15 Leu Thr Ile Ser Val Ile Leu Ala Tyr Ile Ile Val Met Arg Ala Val 20 25 30 Ser Arg Glu Thr Cys Glu Lys Asn Leu Arg Gly Leu Trp Tyr Leu Thr 35 40 45 Ser Ile Gly Ser Arg Cys Val Leu Ala Thr Glu Cys Phe Tyr Arg Gly 50 55 60 Asn Cys Leu Pro Ser Tyr Asp Ala Val Thr Asn Cys Glu Arg Leu Leu 65 70 75 80 Ile Gly Glu Glu Arg Lys Tyr Val Tyr Leu Gln Leu Gly Met Pro Val 85 90 95 Arg Ser Gly Ser Gly His Glu Tyr Phe Asp Gly Gly Ala Met Asn Arg 100 105 110 Ser Glu Leu Ser Val Glu Phe Asn His Asn Arg Leu Val Lys Lys Asn 115 120 125 Cys Arg Phe Glu 130 11 543 DNA Leptospira interrogans serovar copenhageni CDS (1)...(540) 11 atg ttt aga tta aaa ata ttc att tta ctt tgt att tat tct ttt tcc 48 Met Phe Arg Leu Lys Ile Phe Ile Leu Leu Cys Ile Tyr Ser Phe Ser 1 5 10 15 att ttt gca caa tcc aaa gag aaa tgt tta ttc gga gat tgt aag gat 96 Ile Phe Ala Gln Ser Lys Glu Lys Cys Leu Phe Gly Asp Cys Lys Asp 20 25 30 gga aga ggt att ttt ata gac atc cat gga aac gaa ttc ggc gga gtt 144 Gly Arg Gly Ile Phe Ile Asp Ile His Gly Asn Glu Phe Gly Gly Val 35 40 45 ttc gta aac gga aag tta gaa gga gtg ggt gaa atc aaa ttt aaa aac 192 Phe Val Asn Gly Lys Leu Glu Gly Val Gly Glu Ile Lys Phe Lys Asn 50 55 60 gac gga aaa ttt tcc ggc gtt tat aaa aat ccc tca tac cgt gga aaa 240 Asp Gly Lys Phe Ser Gly Val Tyr Lys Asn Pro Ser Tyr Arg Gly Lys 65 70 75 80 tct aaa ttc att gat tca gat gga aaa gtt gta tat gga acc gag ttt 288 Ser Lys Phe Ile Asp Ser Asp Gly Lys Val Val Tyr Gly Thr Glu Phe 85 90 95 acg ggt gga tct tgt ggt gac tac gga tgt gaa act tgg act aaa ttt 336 Thr Gly Gly Ser Cys Gly Asp Tyr Gly Cys Glu Thr Trp Thr Lys Phe 100 105 110 ata ttc gat tcg aat gtg aaa tgt gtt ttt cta ggg acg ttt caa aac 384 Ile Phe Asp Ser Asn Val Lys Cys Val Phe Leu Gly Thr Phe Gln Asn 115 120 125 ggt caa aaa acc ggg aaa ggt agt tat act tgt gat aac cat gaa cgt 432 Gly Gln Lys Thr Gly Lys Gly Ser Tyr Thr Cys Asp Asn His Glu Arg 130 135 140 ttt gaa gga act tac tca aac gat ttg gcc aat gga atg gga aaa tta 480 Phe Glu Gly Thr Tyr Ser Asn Asp Leu Ala Asn Gly Met Gly Lys Leu 145 150 155 160 acc tat tcc gat gga acc att tgg gaa gga aaa ttt aaa aac ggt cat 528 Thr Tyr Ser Asp Gly Thr Ile Trp Glu Gly Lys Phe Lys Asn Gly His 165 170 175 ccg gtt cgg aaa tga 543 Pro Val Arg Lys 180 12 180 PRT Leptospira interrogans serovar copenhageni 12 Met Phe Arg Leu Lys Ile Phe Ile Leu Leu Cys Ile Tyr Ser Phe Ser 1 5 10 15 Ile Phe Ala Gln Ser Lys Glu Lys Cys Leu Phe Gly Asp Cys Lys Asp 20 25 30 Gly Arg Gly Ile Phe Ile Asp Ile His Gly Asn Glu Phe Gly Gly Val 35 40 45 Phe Val Asn Gly Lys Leu Glu Gly Val Gly Glu Ile Lys Phe Lys Asn 50 55 60 Asp Gly Lys Phe Ser Gly Val Tyr Lys Asn Pro Ser Tyr Arg Gly Lys 65 70 75 80 Ser Lys Phe Ile Asp Ser Asp Gly Lys Val Val Tyr Gly Thr Glu Phe 85 90 95 Thr Gly Gly Ser Cys Gly Asp Tyr Gly Cys Glu Thr Trp Thr Lys Phe 100 105 110 Ile Phe Asp Ser Asn Val Lys Cys Val Phe Leu Gly Thr Phe Gln Asn 115 120 125 Gly Gln Lys Thr Gly Lys Gly Ser Tyr Thr Cys Asp Asn His Glu Arg 130 135 140 Phe Glu Gly Thr Tyr Ser Asn Asp Leu Ala Asn Gly Met Gly Lys Leu 145 150 155 160 Thr Tyr Ser Asp Gly Thr Ile Trp Glu Gly Lys Phe Lys Asn Gly His 165 170 175 Pro Val Arg Lys 180 13 612 DNA Leptospira interrogans serovar copenhageni CDS (1)...(609) 13 atg aag aag att aaa att gta aca gtt att act ttg ttt ctg att tct 48 Met Lys Lys Ile Lys Ile Val Thr Val Ile Thr Leu Phe Leu Ile Ser 1 5 10 15 tta act ggt tgt aaa aag agc aaa gaa gaa att gaa aga gaa aag aaa 96 Leu Thr Gly Cys Lys Lys Ser Lys Glu Glu Ile Glu Arg Glu Lys Lys 20 25 30 gaa agt tta aaa aaa gac gtt ctt aat tca ata act atg gtt tat gag 144 Glu Ser Leu Lys Lys Asp Val Leu Asn Ser Ile Thr Met Val Tyr Glu 35 40 45 atg ggc ggc ggc tct act ttt gct ctt ttg gtt gat cca gag aat tat 192 Met Gly Gly Gly Ser Thr Phe Ala Leu Leu Val Asp Pro Glu Asn Tyr 50 55 60 aaa aag gtt gct tgg gct tgt tta gat ttc aaa cct aat gaa aat cga 240 Lys Lys Val Ala Trp Ala Cys Leu Asp Phe Lys Pro Asn Glu Asn Arg 65 70 75 80 gca att ata aaa tat tat aat ttt cct aat cgt tat gaa gtt cgt gtt 288 Ala Ile Ile Lys Tyr Tyr Asn Phe Pro Asn Arg Tyr Glu Val Arg Val 85 90 95 gaa gct att aat gag tta gaa tac aaa tta aat tac agc gat cga gaa 336 Glu Ala Ile Asn Glu Leu Glu Tyr Lys Leu Asn Tyr Ser Asp Arg Glu 100 105 110 gcc agt atg aaa tta gaa gta aca ggt gat tat cct gta aaa gaa ggt 384 Ala Ser Met Lys Leu Glu Val Thr Gly Asp Tyr Pro Val Lys Glu Gly 115 120 125 tct atg gga ttt tta act tcg act gtt tct ctt tct ttt aag ggt gat 432 Ser Met Gly Phe Leu Thr Ser Thr Val Ser Leu Ser Phe Lys Gly Asp 130 135 140 tct aaa gta tat aat gat gtt ggt aga atg gat tta atc tac ggt agt 480 Ser Lys Val Tyr Asn Asp Val Gly Arg Met Asp Leu Ile Tyr Gly Ser 145 150 155 160 gat agt gta gcg aga tcg cgt cat ggt cgt ttt aaa aca tta gaa gaa 528 Asp Ser Val Ala Arg Ser Arg His Gly Arg Phe Lys Thr Leu Glu Glu 165 170 175 tgt gag gct caa ata tct gcg gat gaa gaa cta agc gaa aca ctt cgt 576 Cys Glu Ala Gln Ile Ser Ala Asp Glu Glu Leu Ser Glu Thr Leu Arg 180 185 190 aaa caa gat gga gca tgt gaa ggt cct ggt tgt tag 612 Lys Gln Asp Gly Ala Cys Glu Gly Pro Gly Cys 195 200 14 203 PRT Leptospira interrogans serovar copenhageni 14 Met Lys Lys Ile Lys Ile Val Thr Val Ile Thr Leu Phe Leu Ile Ser 1 5 10 15 Leu Thr Gly Cys Lys Lys Ser Lys Glu Glu Ile Glu Arg Glu Lys Lys 20 25 30 Glu Ser Leu Lys Lys Asp Val Leu Asn Ser Ile Thr Met Val Tyr Glu 35 40 45 Met Gly Gly Gly Ser Thr Phe Ala Leu Leu Val Asp Pro Glu Asn Tyr 50 55 60 Lys Lys Val Ala Trp Ala Cys Leu Asp Phe Lys Pro Asn Glu Asn Arg 65 70 75 80 Ala Ile Ile Lys Tyr Tyr Asn Phe Pro Asn Arg Tyr Glu Val Arg Val 85 90 95 Glu Ala Ile Asn Glu Leu Glu Tyr Lys Leu Asn Tyr Ser Asp Arg Glu 100 105 110 Ala Ser Met Lys Leu Glu Val Thr Gly Asp Tyr Pro Val Lys Glu Gly 115 120 125 Ser Met Gly Phe Leu Thr Ser Thr Val Ser Leu Ser Phe Lys Gly Asp 130 135 140 Ser Lys Val Tyr Asn Asp Val Gly Arg Met Asp Leu Ile Tyr Gly Ser 145 150 155 160 Asp Ser Val Ala Arg Ser Arg His Gly Arg Phe Lys Thr Leu Glu Glu 165 170 175 Cys Glu Ala Gln Ile Ser Ala Asp Glu Glu Leu Ser Glu Thr Leu Arg 180 185 190 Lys Gln Asp Gly Ala Cys Glu Gly Pro Gly Cys 195 200 15 1044 DNA Leptospira interrogans serovar copenhageni CDS (1)...(1041) 15 atg ttt cat ttt aaa acg atc ctg ttt gtt tta act gga ttt att ttt 48 Met Phe His Phe Lys Thr Ile Leu Phe Val Leu Thr Gly Phe Ile Phe 1 5 10 15 ttc gtt tcg gct tgt aaa acg cct cct cct aaa gat ccg tgg atc gtt 96 Phe Val Ser Ala Cys Lys Thr Pro Pro Pro Lys Asp Pro Trp Ile Val 20 25 30 cct tct ctt aaa gag aat gaa aaa cta ttt tta gct cct ttg aaa gtt 144 Pro Ser Leu Lys Glu Asn Glu Lys Leu Phe Leu Ala Pro Leu Lys Val 35 40 45 gat gag ttt gtt tct aaa gat tta gga gga agg cat tat cct gca tcg 192 Asp Glu Phe Val Ser Lys Asp Leu Gly Gly Arg His Tyr Pro Ala Ser 50 55 60 aac gaa ctc aga atc gat ctt ttc aaa ccg tat att gaa aat tta gaa 240 Asn Glu Leu Arg Ile Asp Leu Phe Lys Pro Tyr Ile Glu Asn Leu Glu 65 70 75 80 ggt ggt tat tta ggt gct gga acg gat cag aac ttt aca ttt atc gtt 288 Gly Gly Tyr Leu Gly Ala Gly Thr Asp Gln Asn Phe Thr Phe Ile Val 85 90 95 tgg gca aag agt aaa tat gta tgg tta atg gat ttt gat tat acg att 336 Trp Ala Lys Ser Lys Tyr Val Trp Leu Met Asp Phe Asp Tyr Thr Ile 100 105 110 tgt cta att aat cga att cat ctt ttg ttt ttt aga att gcc gta gat 384 Cys Leu Ile Asn Arg Ile His Leu Leu Phe Phe Arg Ile Ala Val Asp 115 120 125 cct gaa tcg tat cgg gag ctt tgg gct cga aaa aat aaa cat act tct 432 Pro Glu Ser Tyr Arg Glu Leu Trp Ala Arg Lys Asn Lys His Thr Ser 130 135 140 ttt gaa atc ata aag aaa gaa tgg gag aaa gat cca gaa tgg cca ctc 480 Phe Glu Ile Ile Lys Lys Glu Trp Glu Lys Asp Pro Glu Trp Pro Leu 145 150 155 160 att cga gaa gct tgg gaa gtg gct cat aga ggc aaa tca gac gtt cca 528 Ile Arg Glu Ala Trp Glu Val Ala His Arg Gly Lys Ser Asp Val Pro 165 170 175 caa aga tgg aat gag ctt gat cga acg tcg caa aga ttt ggc ctt aag 576 Gln Arg Trp Asn Glu Leu Asp Arg Thr Ser Gln Arg Phe Gly Leu Lys 180 185 190 acg ttt att cat tct aaa gaa gaa tac aat tac att cga aac atg gtt 624 Thr Phe Ile His Ser Lys Glu Glu Tyr Asn Tyr Ile Arg Asn Met Val 195 200 205 ctt caa gga aga ata caa ata tta aaa ggg gac att aat gct gaa aaa 672 Leu Gln Gly Arg Ile Gln Ile Leu Lys Gly Asp Ile Asn Ala Glu Lys 210 215 220 agt atg aga tct gtg gcg gag aga gcc gca aga ttg aac gtt cca att 720 Ser Met Arg Ser Val Ala Glu Arg Ala Ala Arg Leu Asn Val Pro Ile 225 230 235 240 cga gtt gtt tat ctt tct aat ata gaa gac tat ttt tct tac agt gat 768 Arg Val Val Tyr Leu Ser Asn Ile Glu Asp Tyr Phe Ser Tyr Ser Asp 245 250 255 agt ttt cga gac aac cta ctg agt tta ccc acg gat gaa aag gga gtt 816 Ser Phe Arg Asp Asn Leu Leu Ser Leu Pro Thr Asp Glu Lys Gly Val 260 265 270 gtt ttg aga aca atg caa aat gga acc aag gaa gaa tat gga tca cct 864 Val Leu Arg Thr Met Gln Asn Gly Thr Lys Glu Glu Tyr Gly Ser Pro 275 280 285 gac gga gaa aaa att ccg gtg gat tat cct tta cat tat aat gtt caa 912 Asp Gly Glu Lys Ile Pro Val Asp Tyr Pro Leu His Tyr Asn Val Gln 290 295 300 cct ctg gaa aat ttg cag gat tgg atg tta tta tct ggt cat ctt cat 960 Pro Leu Glu Asn Leu Gln Asp Trp Met Leu Leu Ser Gly His Leu His 305 310 315 320 aag gga atc cta atg caa ttc aga act cct att caa aaa ggt ttt tct 1008 Lys Gly Ile Leu Met Gln Phe Arg Thr Pro Ile Gln Lys Gly Phe Ser 325 330 335 ata atc aaa agt ggg ccc gta gaa gtt ttg aaa tga 1044 Ile Ile Lys Ser Gly Pro Val Glu Val Leu Lys 340 345 16 347 PRT Leptospira interrogans serovar copenhageni 16 Met Phe His Phe Lys Thr Ile Leu Phe Val Leu Thr Gly Phe Ile Phe 1 5 10 15 Phe Val Ser Ala Cys Lys Thr Pro Pro Pro Lys Asp Pro Trp Ile Val 20 25 30 Pro Ser Leu Lys Glu Asn Glu Lys Leu Phe Leu Ala Pro Leu Lys Val 35 40 45 Asp Glu Phe Val Ser Lys Asp Leu Gly Gly Arg His Tyr Pro Ala Ser 50 55 60 Asn Glu Leu Arg Ile Asp Leu Phe Lys Pro Tyr Ile Glu Asn Leu Glu 65 70 75 80 Gly Gly Tyr Leu Gly Ala Gly Thr Asp Gln Asn Phe Thr Phe Ile Val 85 90 95 Trp Ala Lys Ser Lys Tyr Val Trp Leu Met Asp Phe Asp Tyr Thr Ile 100 105 110 Cys Leu Ile Asn Arg Ile His Leu Leu Phe Phe Arg Ile Ala Val Asp 115 120 125 Pro Glu Ser Tyr Arg Glu Leu Trp Ala Arg Lys Asn Lys His Thr Ser 130 135 140 Phe Glu Ile Ile Lys Lys Glu Trp Glu Lys Asp Pro Glu Trp Pro Leu 145 150 155 160 Ile Arg Glu Ala Trp Glu Val Ala His Arg Gly Lys Ser Asp Val Pro 165 170 175 Gln Arg Trp Asn Glu Leu Asp Arg Thr Ser Gln Arg Phe Gly Leu Lys 180 185 190 Thr Phe Ile His Ser Lys Glu Glu Tyr Asn Tyr Ile Arg Asn Met Val 195 200 205 Leu Gln Gly Arg Ile Gln Ile Leu Lys Gly Asp Ile Asn Ala Glu Lys 210 215 220 Ser Met Arg Ser Val Ala Glu Arg Ala Ala Arg Leu Asn Val Pro Ile 225 230 235 240 Arg Val Val Tyr Leu Ser Asn Ile Glu Asp Tyr Phe Ser Tyr Ser Asp 245 250 255 Ser Phe Arg Asp Asn Leu Leu Ser Leu Pro Thr Asp Glu Lys Gly Val 260 265 270 Val Leu Arg Thr Met Gln Asn Gly Thr Lys Glu Glu Tyr Gly Ser Pro 275 280 285 Asp Gly Glu Lys Ile Pro Val Asp Tyr Pro Leu His Tyr Asn Val Gln 290 295 300 Pro Leu Glu Asn Leu Gln Asp Trp Met Leu Leu Ser Gly His Leu His 305 310 315 320 Lys Gly Ile Leu Met Gln Phe Arg Thr Pro Ile Gln Lys Gly Phe Ser 325 330 335 Ile Ile Lys Ser Gly Pro Val Glu Val Leu Lys 340 345 17 576 DNA Leptospira interrogans serovar copenhageni CDS (1)...(573) 17 atg ttc aaa ata tta gta aaa att aat att cta ttt ttc ttt tta gtt 48 Met Phe Lys Ile Leu Val Lys Ile Asn Ile Leu Phe Phe Phe Leu Val 1 5 10 15 tat ttt tta ttg ttt ggg tgt tgt gct cct tcg agg ttg gaa atc gtt 96 Tyr Phe Leu Leu Phe Gly Cys Cys Ala Pro Ser Arg Leu Glu Ile Val 20 25 30 tct atg att ctt tgt gat cat ttc aat cgg gtt gga gaa tgt ctc gaa 144 Ser Met Ile Leu Cys Asp His Phe Asn Arg Val Gly Glu Cys Leu Glu 35 40 45 cct gtg gaa aga aat cat cat tat aaa ata gaa att cca aat cac aaa 192 Pro Val Glu Arg Asn His His Tyr Lys Ile Glu Ile Pro Asn His Lys 50 55 60 aaa ccg gat act tgg gaa aag ttt tct aat tat ctt tac ttt cat gcg 240 Lys Pro Asp Thr Trp Glu Lys Phe Ser Asn Tyr Leu Tyr Phe His Ala 65 70 75 80 aga gaa act cct ggt ttt ctg att cga ttt aat cga aag ttg act cct 288 Arg Glu Thr Pro Gly Phe Leu Ile Arg Phe Asn Arg Lys Leu Thr Pro 85 90 95 tcc gaa tct aaa atg atc aaa gat tct tat tac gcc acg atg agt ttt 336 Ser Glu Ser Lys Met Ile Lys Asp Ser Tyr Tyr Ala Thr Met Ser Phe 100 105 110 tcc gga act gta gaa agg atg gaa ggt ttt gaa atg gga gaa gat tgg 384 Ser Gly Thr Val Glu Arg Met Glu Gly Phe Glu Met Gly Glu Asp Trp 115 120 125 gtt ggt tcg ttt cag tat ctg ggt tct ata att aaa gaa aaa tta aaa 432 Val Gly Ser Phe Gln Tyr Leu Gly Ser Ile Ile Lys Glu Lys Leu Lys 130 135 140 aaa gaa aat cgc ctc tct tcc ttt cct tat aca aat tct atc ttt ccg 480 Lys Glu Asn Arg Leu Ser Ser Phe Pro Tyr Thr Asn Ser Ile Phe Pro 145 150 155 160 gca gaa gtg gaa ttt aga ttc aat tct tct ctt ttt gaa ggg gaa gaa 528 Ala Glu Val Glu Phe Arg Phe Asn Ser Ser Leu Phe Glu Gly Glu Glu 165 170 175 aaa acg aaa att aat cta agt ttt atc gtt ctt cct cca gaa aaa tga 576 Lys Thr Lys Ile Asn Leu Ser Phe Ile Val Leu Pro Pro Glu Lys 180 185 190 18 191 PRT Leptospira interrogans serovar copenhageni 18 Met Phe Lys Ile Leu Val Lys Ile Asn Ile Leu Phe Phe Phe Leu Val 1 5 10 15 Tyr Phe Leu Leu Phe Gly Cys Cys Ala Pro Ser Arg Leu Glu Ile Val 20 25 30 Ser Met Ile Leu Cys Asp His Phe Asn Arg Val Gly Glu Cys Leu Glu 35 40 45 Pro Val Glu Arg Asn His His Tyr Lys Ile Glu Ile Pro Asn His Lys 50 55 60 Lys Pro Asp Thr Trp Glu Lys Phe Ser Asn Tyr Leu Tyr Phe His Ala 65 70 75 80 Arg Glu Thr Pro Gly Phe Leu Ile Arg Phe Asn Arg Lys Leu Thr Pro 85 90 95 Ser Glu Ser Lys Met Ile Lys Asp Ser Tyr Tyr Ala Thr Met Ser Phe 100 105 110 Ser Gly Thr Val Glu Arg Met Glu Gly Phe Glu Met Gly Glu Asp Trp 115 120 125 Val Gly Ser Phe Gln Tyr Leu Gly Ser Ile Ile Lys Glu Lys Leu Lys 130 135 140 Lys Glu Asn Arg Leu Ser Ser Phe Pro Tyr Thr Asn Ser Ile Phe Pro 145 150 155 160 Ala Glu Val Glu Phe Arg Phe Asn Ser Ser Leu Phe Glu Gly Glu Glu 165 170 175 Lys Thr Lys Ile Asn Leu Ser Phe Ile Val Leu Pro Pro Glu Lys 180 185 190 19 483 DNA Leptospira interrogans serovar copenhageni CDS (1)...(480) 19 atg aag aaa tta ttc gtt att gct ctg gct ctc ttt atg gtt tct aac 48 Met Lys Lys Leu Phe Val Ile Ala Leu Ala Leu Phe Met Val Ser Asn 1 5 10 15 ctt tct gca aaa cct gga tat gga atg gcg gga tgc ggt tta gga tct 96 Leu Ser Ala Lys Pro Gly Tyr Gly Met Ala Gly Cys Gly Leu Gly Ser 20 25 30 ata atc att aaa gat aat ggt ttt gtg caa att ttt gca act acc tca 144 Ile Ile Ile Lys Asp Asn Gly Phe Val Gln Ile Phe Ala Thr Thr Ser 35 40 45 aat cta act tct tac aat caa act ttt gga att act tct ggc act tcc 192 Asn Leu Thr Ser Tyr Asn Gln Thr Phe Gly Ile Thr Ser Gly Thr Ser 50 55 60 aat tgc agt tca gat gga atc gtg aac aat gac aaa gca aag gaa att 240 Asn Cys Ser Ser Asp Gly Ile Val Asn Asn Asp Lys Ala Lys Glu Ile 65 70 75 80 ttt gtt cat atg aac tac gaa agt ctt gaa caa gaa att gca atg gga 288 Phe Val His Met Asn Tyr Glu Ser Leu Glu Gln Glu Ile Ala Met Gly 85 90 95 aaa gga gag aaa ctt tcc agt tta gct gca ctt ttt gga tgt tct aac 336 Lys Gly Glu Lys Leu Ser Ser Leu Ala Ala Leu Phe Gly Cys Ser Asn 100 105 110 gat tct aaa aga ttt aaa gaa gtt gct aaa gaa aat ttc tct aaa att 384 Asp Ser Lys Arg Phe Lys Glu Val Ala Lys Glu Asn Phe Ser Lys Ile 115 120 125 ttc acg acg gca gca att aaa aat ccg act gta atg ctt tct aat tta 432 Phe Thr Thr Ala Ala Ile Lys Asn Pro Thr Val Met Leu Ser Asn Leu 130 135 140 gaa ttg gaa gtt gga aaa gat aca gaa tta aag aac agc tgt aaa atc 480 Glu Leu Glu Val Gly Lys Asp Thr Glu Leu Lys Asn Ser Cys Lys Ile 145 150 155 160 taa 483 20 160 PRT Leptospira interrogans serovar copenhageni 20 Met Lys Lys Leu Phe Val Ile Ala Leu Ala Leu Phe Met Val Ser Asn 1 5 10 15 Leu Ser Ala Lys Pro Gly Tyr Gly Met Ala Gly Cys Gly Leu Gly Ser 20 25 30 Ile Ile Ile Lys Asp Asn Gly Phe Val Gln Ile Phe Ala Thr Thr Ser 35 40 45 Asn Leu Thr Ser Tyr Asn Gln Thr Phe Gly Ile Thr Ser Gly Thr Ser 50 55 60 Asn Cys Ser Ser Asp Gly Ile Val Asn Asn Asp Lys Ala Lys Glu Ile 65 70 75 80 Phe Val His Met Asn Tyr Glu Ser Leu Glu Gln Glu Ile Ala Met Gly 85 90 95 Lys Gly Glu Lys Leu Ser Ser Leu Ala Ala Leu Phe Gly Cys Ser Asn 100 105 110 Asp Ser Lys Arg Phe Lys Glu Val Ala Lys Glu Asn Phe Ser Lys Ile 115 120 125 Phe Thr Thr Ala Ala Ile Lys Asn Pro Thr Val Met Leu Ser Asn Leu 130 135 140 Glu Leu Glu Val Gly Lys Asp Thr Glu Leu Lys Asn Ser Cys Lys Ile 145 150 155 160 21 819 DNA Leptospira interrogans serovar copenhageni CDS (1)...(816) 21 atg ttt tcc cgg tgt cga att ttc tta aaa cct acg acc cta att tgg 48 Met Phe Ser Arg Cys Arg Ile Phe Leu Lys Pro Thr Thr Leu Ile Trp 1 5 10 15 ttt gca att ctt ccg gga gcc tta tct gct tct cct caa aaa cca gga 96 Phe Ala Ile Leu Pro Gly Ala Leu Ser Ala Ser Pro Gln Lys Pro Gly 20 25 30 acc ttc gaa ttg tta ggt ggt tac caa ccc aat tgg aat cga ctt ttc 144 Thr Phe Glu Leu Leu Gly Gly Tyr Gln Pro Asn Trp Asn Arg Leu Phe 35 40 45 act gag ttt ctt ccg aaa cgt aca gca caa act ggt aac cta cct tct 192 Thr Glu Phe Leu Pro Lys Arg Thr Ala Gln Thr Gly Asn Leu Pro Ser 50 55 60 agc ggc gtc att tcc aga gaa gaa gag gac ata gaa aat cca gag gaa 240 Ser Gly Val Ile Ser Arg Glu Glu Glu Asp Ile Glu Asn Pro Glu Glu 65 70 75 80 aca gaa gaa gat aaa caa gaa gga tac caa gac aat cga aaa acg gaa 288 Thr Glu Glu Asp Lys Gln Glu Gly Tyr Gln Asp Asn Arg Lys Thr Glu 85 90 95 gtt gga gtt tgg gta gga gct tcc aat ccg tta ccc gga acc gaa act 336 Val Gly Val Trp Val Gly Ala Ser Asn Pro Leu Pro Gly Thr Glu Thr 100 105 110 caa aaa tat ctg gat act acg tta ggt ggc ggt ttc ttt ttt aga att 384 Gln Lys Tyr Leu Asp Thr Thr Leu Gly Gly Gly Phe Phe Phe Arg Ile 115 120 125 ccc tgg cct tgg atc ttt tat ctc gaa atg gga gcc ttt tac gca aat 432 Pro Trp Pro Trp Ile Phe Tyr Leu Glu Met Gly Ala Phe Tyr Ala Asn 130 135 140 tat ctt tcg gca aca gaa aga gct ttg act aca att ccg gtc tat ctt 480 Tyr Leu Ser Ala Thr Glu Arg Ala Leu Thr Thr Ile Pro Val Tyr Leu 145 150 155 160 gct ttg ggt tat aaa att cct tta gat ctt cca att tcg ttt atc ctt 528 Ala Leu Gly Tyr Lys Ile Pro Leu Asp Leu Pro Ile Ser Phe Ile Leu 165 170 175 cgt gcg gga ggt gga gaa gcg ttt gta gta gca aga cct tcc aac aca 576 Arg Ala Gly Gly Gly Glu Ala Phe Val Val Ala Arg Pro Ser Asn Thr 180 185 190 tct cgt tgg gat cca atg atg att gta gga tta gaa act agt ttt gta 624 Ser Arg Trp Asp Pro Met Met Ile Val Gly Leu Glu Thr Ser Phe Val 195 200 205 gct gga aaa aaa atc cga atc gga att cga atc gat tac aat aaa att 672 Ala Gly Lys Lys Ile Arg Ile Gly Ile Arg Ile Asp Tyr Asn Lys Ile 210 215 220 tat gag tct cgt atg gac gcc cca gga gaa aca aaa tat cct tac acg 720 Tyr Glu Ser Arg Met Asp Ala Pro Gly Glu Thr Lys Tyr Pro Tyr Thr 225 230 235 240 agt cct tac gaa gat tcc aga ttg agt aac ccc aat tat tac aga gta 768 Ser Pro Tyr Glu Asp Ser Arg Leu Ser Asn Pro Asn Tyr Tyr Arg Val 245 250 255 gta gat act gaa ttt ttt cag ttc ggt ttg atg gtg agt gta ttt tta 816 Val Asp Thr Glu Phe Phe Gln Phe Gly Leu Met Val Ser Val Phe Leu 260 265 270 tga 819 22 272 PRT Leptospira interrogans serovar copenhageni 22 Met Phe Ser Arg Cys Arg Ile Phe Leu Lys Pro Thr Thr Leu Ile Trp 1 5 10 15 Phe Ala Ile Leu Pro Gly Ala Leu Ser Ala Ser Pro Gln Lys Pro Gly 20 25 30 Thr Phe Glu Leu Leu Gly Gly Tyr Gln Pro Asn Trp Asn Arg Leu Phe 35 40 45 Thr Glu Phe Leu Pro Lys Arg Thr Ala Gln Thr Gly Asn Leu Pro Ser 50 55 60 Ser Gly Val Ile Ser Arg Glu Glu Glu Asp Ile Glu Asn Pro Glu Glu 65 70 75 80 Thr Glu Glu Asp Lys Gln Glu Gly Tyr Gln Asp Asn Arg Lys Thr Glu 85 90 95 Val Gly Val Trp Val Gly Ala Ser Asn Pro Leu Pro Gly Thr Glu Thr 100 105 110 Gln Lys Tyr Leu Asp Thr Thr Leu Gly Gly Gly Phe Phe Phe Arg Ile 115 120 125 Pro Trp Pro Trp Ile Phe Tyr Leu Glu Met Gly Ala Phe Tyr Ala Asn 130 135 140 Tyr Leu Ser Ala Thr Glu Arg Ala Leu Thr Thr Ile Pro Val Tyr Leu 145 150 155 160 Ala Leu Gly Tyr Lys Ile Pro Leu Asp Leu Pro Ile Ser Phe Ile Leu 165 170 175 Arg Ala Gly Gly Gly Glu Ala Phe Val Val Ala Arg Pro Ser Asn Thr 180 185 190 Ser Arg Trp Asp Pro Met Met Ile Val Gly Leu Glu Thr Ser Phe Val 195 200 205 Ala Gly Lys Lys Ile Arg Ile Gly Ile Arg Ile Asp Tyr Asn Lys Ile 210 215 220 Tyr Glu Ser Arg Met Asp Ala Pro Gly Glu Thr Lys Tyr Pro Tyr Thr 225 230 235 240 Ser Pro Tyr Glu Asp Ser Arg Leu Ser Asn Pro Asn Tyr Tyr Arg Val 245 250 255 Val Asp Thr Glu Phe Phe Gln Phe Gly Leu Met Val Ser Val Phe Leu 260 265 270 23 729 DNA Leptospira interrogans serovar copenhageni CDS (1)...(726) 23 atg aat tac aaa ata aga ata tta ttt ctt atc att tta ctt tcg gct 48 Met Asn Tyr Lys Ile Arg Ile Leu Phe Leu Ile Ile Leu Leu Ser Ala 1 5 10 15 ata gca agc tcg atc aca ctc ctg agc cag gaa acg gaa aac gct aaa 96 Ile Ala Ser Ser Ile Thr Leu Leu Ser Gln Glu Thr Glu Asn Ala Lys 20 25 30 gta agt ttt tca tta ggt aaa tct tat gtt caa aaa tct ggt aaa agc 144 Val Ser Phe Ser Leu Gly Lys Ser Tyr Val Gln Lys Ser Gly Lys Ser 35 40 45 tcc tgg gaa cct tta aaa cca aac gat ttt ttg gaa gaa gga gat tta 192 Ser Trp Glu Pro Leu Lys Pro Asn Asp Phe Leu Glu Glu Gly Asp Leu 50 55 60 atc tcc acc gga aac ggt tct aga att acg gtt cat tac aaa ggt tcc 240 Ile Ser Thr Gly Asn Gly Ser Arg Ile Thr Val His Tyr Lys Gly Ser 65 70 75 80 gaa ttt aag att caa caa aac agc aaa gta aaa ctt tca aac ctt cct 288 Glu Phe Lys Ile Gln Gln Asn Ser Lys Val Lys Leu Ser Asn Leu Pro 85 90 95 gaa aaa tct aaa cga ggt gta tta gaa gta aat caa ggt ttc gca tgg 336 Glu Lys Ser Lys Arg Gly Val Leu Glu Val Asn Gln Gly Phe Ala Trp 100 105 110 ttt aag atc gta aat ctc aaa ggg aaa aaa ttt gaa gtt aca aca cca 384 Phe Lys Ile Val Asn Leu Lys Gly Lys Lys Phe Glu Val Thr Thr Pro 115 120 125 aat tcc acg gcg gga gtc aga ggc act tca ttt tct gct ttc tac gat 432 Asn Ser Thr Ala Gly Val Arg Gly Thr Ser Phe Ser Ala Phe Tyr Asp 130 135 140 cct aaa aca aga gaa tcg tct ttt tgc act tgc gaa ggc aag gta tct 480 Pro Lys Thr Arg Glu Ser Ser Phe Cys Thr Cys Glu Gly Lys Val Ser 145 150 155 160 att tcc gat tct aca gga aaa gaa att ctt ttt caa gaa aaa ggc gaa 528 Ile Ser Asp Ser Thr Gly Lys Glu Ile Leu Phe Gln Glu Lys Gly Glu 165 170 175 ggt aca atc gtc tct tca aaa gat ata gaa att aaa aaa ttt gaa tat 576 Gly Thr Ile Val Ser Ser Lys Asp Ile Glu Ile Lys Lys Phe Glu Tyr 180 185 190 aaa gga att att aaa aaa tta aat acc cta tct ggc ttt gaa gag agg 624 Lys Gly Ile Ile Lys Lys Leu Asn Thr Leu Ser Gly Phe Glu Glu Arg 195 200 205 cta aaa aaa aat cct ttt tta aaa aac tgt ctt tct tgt cac act cca 672 Leu Lys Lys Asn Pro Phe Leu Lys Asn Cys Leu Ser Cys His Thr Pro 210 215 220 gag ggt tgg att cca caa gaa gaa act ctt aag gac gaa acc tac ggc 720 Glu Gly Trp Ile Pro Gln Glu Glu Thr Leu Lys Asp Glu Thr Tyr Gly 225 230 235 240 aaa caa taa 729 Lys Gln 24 242 PRT Leptospira interrogans serovar copenhageni 24 Met Asn Tyr Lys Ile Arg Ile Leu Phe Leu Ile Ile Leu Leu Ser Ala 1 5 10 15 Ile Ala Ser Ser Ile Thr Leu Leu Ser Gln Glu Thr Glu Asn Ala Lys 20 25 30 Val Ser Phe Ser Leu Gly Lys Ser Tyr Val Gln Lys Ser Gly Lys Ser 35 40 45 Ser Trp Glu Pro Leu Lys Pro Asn Asp Phe Leu Glu Glu Gly Asp Leu 50 55 60 Ile Ser Thr Gly Asn Gly Ser Arg Ile Thr Val His Tyr Lys Gly Ser 65 70 75 80 Glu Phe Lys Ile Gln Gln Asn Ser Lys Val Lys Leu Ser Asn Leu Pro 85 90 95 Glu Lys Ser Lys Arg Gly Val Leu Glu Val Asn Gln Gly Phe Ala Trp 100 105 110 Phe Lys Ile Val Asn Leu Lys Gly Lys Lys Phe Glu Val Thr Thr Pro 115 120 125 Asn Ser Thr Ala Gly Val Arg Gly Thr Ser Phe Ser Ala Phe Tyr Asp 130 135 140 Pro Lys Thr Arg Glu Ser Ser Phe Cys Thr Cys Glu Gly Lys Val Ser 145 150 155 160 Ile Ser Asp Ser Thr Gly Lys Glu Ile Leu Phe Gln Glu Lys Gly Glu 165 170 175 Gly Thr Ile Val Ser Ser Lys Asp Ile Glu Ile Lys Lys Phe Glu Tyr 180 185 190 Lys Gly Ile Ile Lys Lys Leu Asn Thr Leu Ser Gly Phe Glu Glu Arg 195 200 205 Leu Lys Lys Asn Pro Phe Leu Lys Asn Cys Leu Ser Cys His Thr Pro 210 215 220 Glu Gly Trp Ile Pro Gln Glu Glu Thr Leu Lys Asp Glu Thr Tyr Gly 225 230 235 240 Lys Gln 25 546 DNA Leptospira interrogans serovar copenhageni CDS (1)...(543) 25 atg aaa att ttt gca ctg agt att tta gtt tta gta gtt tta ctt gta 48 Met Lys Ile Phe Ala Leu Ser Ile Leu Val Leu Val Val Leu Leu Val 1 5 10 15 gcg ttc ttg ttt tat atg ggc gct ttt aat cgg gtt ttg gtt caa gag 96 Ala Phe Leu Phe Tyr Met Gly Ala Phe Asn Arg Val Leu Val Gln Glu 20 25 30 gaa atg aaa gga ccg ttt tac gtt ctt tcg cat gaa agg att gga gat 144 Glu Met Lys Gly Pro Phe Tyr Val Leu Ser His Glu Arg Ile Gly Asp 35 40 45 tat aga aac gtt ggg ctt acg ttt gaa gcc ctt caa aaa gaa ctg cct 192 Tyr Arg Asn Val Gly Leu Thr Phe Glu Ala Leu Gln Lys Glu Leu Pro 50 55 60 gaa aaa gga att cga aat ttt aaa ttg ttc tca ata tat ttg gat aat 240 Glu Lys Gly Ile Arg Asn Phe Lys Leu Phe Ser Ile Tyr Leu Asp Asn 65 70 75 80 cca aat gag gtt cct aaa gaa aaa cta cga tgt gaa gta gga gct ctt 288 Pro Asn Glu Val Pro Lys Glu Lys Leu Arg Cys Glu Val Gly Ala Leu 85 90 95 ttt tcg gaa cca tta gaa aaa att cca aat gga ctt tct tta gag tta 336 Phe Ser Glu Pro Leu Glu Lys Ile Pro Asn Gly Leu Ser Leu Glu Leu 100 105 110 aaa ata aga acc att cct tct aaa aaa tat ctt acc gcg gaa ttt cca 384 Lys Ile Arg Thr Ile Pro Ser Lys Lys Tyr Leu Thr Ala Glu Phe Pro 115 120 125 ttg aga aat ttt ctt tct att ttt ctt gga att tat aag gtt tat ccg 432 Leu Arg Asn Phe Leu Ser Ile Phe Leu Gly Ile Tyr Lys Val Tyr Pro 130 135 140 aaa ctt ttc aga gcc tgt gaa gaa aga ggt tgt gat ctt aaa gga agg 480 Lys Leu Phe Arg Ala Cys Glu Glu Arg Gly Cys Asp Leu Lys Gly Arg 145 150 155 160 gca tcc att gaa att tat gaa cct ctt acg gaa cat aag act aca tat 528 Ala Ser Ile Glu Ile Tyr Glu Pro Leu Thr Glu His Lys Thr Thr Tyr 165 170 175 ctt ctg cct tta gat tag 546 Leu Leu Pro Leu Asp 180 26 181 PRT Leptospira interrogans serovar copenhageni 26 Met Lys Ile Phe Ala Leu Ser Ile Leu Val Leu Val Val Leu Leu Val 1 5 10 15 Ala Phe Leu Phe Tyr Met Gly Ala Phe Asn Arg Val Leu Val Gln Glu 20 25 30 Glu Met Lys Gly Pro Phe Tyr Val Leu Ser His Glu Arg Ile Gly Asp 35 40 45 Tyr Arg Asn Val Gly Leu Thr Phe Glu Ala Leu Gln Lys Glu Leu Pro 50 55 60 Glu Lys Gly Ile Arg Asn Phe Lys Leu Phe Ser Ile Tyr Leu Asp Asn 65 70 75 80 Pro Asn Glu Val Pro Lys Glu Lys Leu Arg Cys Glu Val Gly Ala Leu 85 90 95 Phe Ser Glu Pro Leu Glu Lys Ile Pro Asn Gly Leu Ser Leu Glu Leu 100 105 110 Lys Ile Arg Thr Ile Pro Ser Lys Lys Tyr Leu Thr Ala Glu Phe Pro 115 120 125 Leu Arg Asn Phe Leu Ser Ile Phe Leu Gly Ile Tyr Lys Val Tyr Pro 130 135 140 Lys Leu Phe Arg Ala Cys Glu Glu Arg Gly Cys Asp Leu Lys Gly Arg 145 150 155 160 Ala Ser Ile Glu Ile Tyr Glu Pro Leu Thr Glu His Lys Thr Thr Tyr 165 170 175 Leu Leu Pro Leu Asp 180 27 570 DNA Leptospira interrogans serovar copenhageni CDS (1)...(567) 27 atg aag gtt aaa aat atc cgg aaa gga ttt acc ctg atc gag ttg atc 48 Met Lys Val Lys Asn Ile Arg Lys Gly Phe Thr Leu Ile Glu Leu Ile 1 5 10 15 gtg gtt atc gcg atc ctc gcg ggg tta att agt att ctt gca agt acc 96 Val Val Ile Ala Ile Leu Ala Gly Leu Ile Ser Ile Leu Ala Ser Thr 20 25 30 gct gca aac ttt atc att cct tcg gga agt gac gcg gca caa act tta 144 Ala Ala Asn Phe Ile Ile Pro Ser Gly Ser Asp Ala Ala Gln Thr Leu 35 40 45 aaa caa gcc gct gaa ttc tgt tat cga aaa tcc att ctt aca aac acc 192 Lys Gln Ala Ala Glu Phe Cys Tyr Arg Lys Ser Ile Leu Thr Asn Thr 50 55 60 act atg gtt tta gaa ctg gat ata gac aac gat acc tat tct atc aaa 240 Thr Met Val Leu Glu Leu Asp Ile Asp Asn Asp Thr Tyr Ser Ile Lys 65 70 75 80 aaa tta ctt cga gac gaa agt gga att aaa gaa gtt ttg gtt ttt aaa 288 Lys Leu Leu Arg Asp Glu Ser Gly Ile Lys Glu Val Leu Val Phe Lys 85 90 95 cct cag aaa ctt cct tat act tcc gaa att ata gat ata act gat att 336 Pro Gln Lys Leu Pro Tyr Thr Ser Glu Ile Ile Asp Ile Thr Asp Ile 100 105 110 aga ggt ttt aga tat acg aaa gga att att aaa gtt ccc tat acc tat 384 Arg Gly Phe Arg Tyr Thr Lys Gly Ile Ile Lys Val Pro Tyr Thr Tyr 115 120 125 ctt ggg atc tcg gca gac tac agt gta cat tta gga agt gat cct tcc 432 Leu Gly Ile Ser Ala Asp Tyr Ser Val His Leu Gly Ser Asp Pro Ser 130 135 140 att tat aga act ttg att ctt tat aga tac ggc gga aag gtt tcc gtt 480 Ile Tyr Arg Thr Leu Ile Leu Tyr Arg Tyr Gly Gly Lys Val Ser Val 145 150 155 160 gtg gaa gga gag cag ttt cat act tct tcg aat ttg gca acc gat aaa 528 Val Glu Gly Glu Gln Phe His Thr Ser Ser Asn Leu Ala Thr Asp Lys 165 170 175 aat tgg aaa gaa cag gat gat aac gaa caa caa cag cct taa 570 Asn Trp Lys Glu Gln Asp Asp Asn Glu Gln Gln Gln Pro 180 185 28 189 PRT Leptospira interrogans serovar copenhageni 28 Met Lys Val Lys Asn Ile Arg Lys Gly Phe Thr Leu Ile Glu Leu Ile 1 5 10 15 Val Val Ile Ala Ile Leu Ala Gly Leu Ile Ser Ile Leu Ala Ser Thr 20 25 30 Ala Ala Asn Phe Ile Ile Pro Ser Gly Ser Asp Ala Ala Gln Thr Leu 35 40 45 Lys Gln Ala Ala Glu Phe Cys Tyr Arg Lys Ser Ile Leu Thr Asn Thr 50 55 60 Thr Met Val Leu Glu Leu Asp Ile Asp Asn Asp Thr Tyr Ser Ile Lys 65 70 75 80 Lys Leu Leu Arg Asp Glu Ser Gly Ile Lys Glu Val Leu Val Phe Lys 85 90 95 Pro Gln Lys Leu Pro Tyr Thr Ser Glu Ile Ile Asp Ile Thr Asp Ile 100 105 110 Arg Gly Phe Arg Tyr Thr Lys Gly Ile Ile Lys Val Pro Tyr Thr Tyr 115 120 125 Leu Gly Ile Ser Ala Asp Tyr Ser Val His Leu Gly Ser Asp Pro Ser 130 135 140 Ile Tyr Arg Thr Leu Ile Leu Tyr Arg Tyr Gly Gly Lys Val Ser Val 145 150 155 160 Val Glu Gly Glu Gln Phe His Thr Ser Ser Asn Leu Ala Thr Asp Lys 165 170 175 Asn Trp Lys Glu Gln Asp Asp Asn Glu Gln Gln Gln Pro 180 185 29 441 DNA Leptospira interrogans serovar copenhageni CDS (1)...(438) 29 atg aag aat tct ttt cat aaa caa aac cgc aag gaa tcc tgt caa aat 48 Met Lys Asn Ser Phe His Lys Gln Asn Arg Lys Glu Ser Cys Gln Asn 1 5 10 15 agt atg aaa aag tta tta ctc gtt tgt gtt tta gta tgt ttt gtt ggg 96 Ser Met Lys Lys Leu Leu Leu Val Cys Val Leu Val Cys Phe Val Gly 20 25 30 gtt ttt gcc gaa gaa gaa agt ccc gta agg ttc aaa ctg gaa aaa agt 144 Val Phe Ala Glu Glu Glu Ser Pro Val Arg Phe Lys Leu Glu Lys Ser 35 40 45 ttt ggt aat gcg tat att tta aaa att att cat ccg gct aac ttc ggt 192 Phe Gly Asn Ala Tyr Ile Leu Lys Ile Ile His Pro Ala Asn Phe Gly 50 55 60 gtt caa aag gac gct cct cat aaa ata att tta aat cct agg aac gga 240 Val Gln Lys Asp Ala Pro His Lys Ile Ile Leu Asn Pro Arg Asn Gly 65 70 75 80 gta aag gtt gaa aaa gcg gat ctg aaa gta aaa gga aaa att tca gaa 288 Val Lys Val Glu Lys Ala Asp Leu Lys Val Lys Gly Lys Ile Ser Glu 85 90 95 aag aaa aaa gaa tat ttt gcc tcg gtg gat ccg att tct ctt gtt gtg 336 Lys Lys Lys Glu Tyr Phe Ala Ser Val Asp Pro Ile Ser Leu Val Val 100 105 110 act ggt aaa gga gaa ttg gag att caa gga aag att tac tac tgt aac 384 Thr Gly Lys Gly Glu Leu Glu Ile Gln Gly Lys Ile Tyr Tyr Cys Asn 115 120 125 ttt gat aaa aat atc tgc att cca ggt aag att cag caa gta gag atc 432 Phe Asp Lys Asn Ile Cys Ile Pro Gly Lys Ile Gln Gln Val Glu Ile 130 135 140 att caa taa 441 Ile Gln 145 30 146 PRT Leptospira interrogans serovar copenhageni 30 Met Lys Asn Ser Phe His Lys Gln Asn Arg Lys Glu Ser Cys Gln Asn 1 5 10 15 Ser Met Lys Lys Leu Leu Leu Val Cys Val Leu Val Cys Phe Val Gly 20 25 30 Val Phe Ala Glu Glu Glu Ser Pro Val Arg Phe Lys Leu Glu Lys Ser 35 40 45 Phe Gly Asn Ala Tyr Ile Leu Lys Ile Ile His Pro Ala Asn Phe Gly 50 55 60 Val Gln Lys Asp Ala Pro His Lys Ile Ile Leu Asn Pro Arg Asn Gly 65 70 75 80 Val Lys Val Glu Lys Ala Asp Leu Lys Val Lys Gly Lys Ile Ser Glu 85 90 95 Lys Lys Lys Glu Tyr Phe Ala Ser Val Asp Pro Ile Ser Leu Val Val 100 105 110 Thr Gly Lys Gly Glu Leu Glu Ile Gln Gly Lys Ile Tyr Tyr Cys Asn 115 120 125 Phe Asp Lys Asn Ile Cys Ile Pro Gly Lys Ile Gln Gln Val Glu Ile 130 135 140 Ile Gln 145 31 546 DNA Leptospira interrogans serovar copenhageni CDS (1)...(543) 31 atg aaa cat ttt aac caa ctc gtt ttg tcg ttt ttg att ttt ttt acg 48 Met Lys His Phe Asn Gln Leu Val Leu Ser Phe Leu Ile Phe Phe Thr 1 5 10 15 tct caa agt tac gct tca gag atc ctt aaa aaa gaa atc act ttt tta 96 Ser Gln Ser Tyr Ala Ser Glu Ile Leu Lys Lys Glu Ile Thr Phe Leu 20 25 30 gca att cat cct atg aaa gaa gtt cat gga gct tgt aag gag ata caa 144 Ala Ile His Pro Met Lys Glu Val His Gly Ala Cys Lys Glu Ile Gln 35 40 45 gta gat tct cct caa att caa acg agc gga acc gtt tat aaa ttg aat 192 Val Asp Ser Pro Gln Ile Gln Thr Ser Gly Thr Val Tyr Lys Leu Asn 50 55 60 tct cct ttt aca att aaa att ccg att ttg aaa att cat tcg gga gat 240 Ser Pro Phe Thr Ile Lys Ile Pro Ile Leu Lys Ile His Ser Gly Asp 65 70 75 80 gaa aac aga gac tct cat atc atg gaa att tta ggt tat cct gat att 288 Glu Asn Arg Asp Ser His Ile Met Glu Ile Leu Gly Tyr Pro Asp Ile 85 90 95 ccg gaa att ata gtt gtc gta gaa tcc gcc gaa gcc gtt ggt gaa acg 336 Pro Glu Ile Ile Val Val Val Glu Ser Ala Glu Ala Val Gly Glu Thr 100 105 110 tat tta att cgt ggt aaa ctt tcg att cac gga ttt act cgc gac ttt 384 Tyr Leu Ile Arg Gly Lys Leu Ser Ile His Gly Phe Thr Arg Asp Phe 115 120 125 caa tct tct gga aaa gtt gag cca aat ggg gtg ggt cag att cgt ata 432 Gln Ser Ser Gly Lys Val Glu Pro Asn Gly Val Gly Gln Ile Arg Ile 130 135 140 ttt gga aaa gtg aat att caa ttt tcc gat ttt aat ctc gaa aga ccc 480 Phe Gly Lys Val Asn Ile Gln Phe Ser Asp Phe Asn Leu Glu Arg Pro 145 150 155 160 tct ctt tta ttt ata aaa aca aaa gaa gaa att gaa att gga tat gat 528 Ser Leu Leu Phe Ile Lys Thr Lys Glu Glu Ile Glu Ile Gly Tyr Asp 165 170 175 ttt tta att aag ata taa 546 Phe Leu Ile Lys Ile 180 32 181 PRT Leptospira interrogans serovar copenhageni 32 Met Lys His Phe Asn Gln Leu Val Leu Ser Phe Leu Ile Phe Phe Thr 1 5 10 15 Ser Gln Ser Tyr Ala Ser Glu Ile Leu Lys Lys Glu Ile Thr Phe Leu 20 25 30 Ala Ile His Pro Met Lys Glu Val His Gly Ala Cys Lys Glu Ile Gln 35 40 45 Val Asp Ser Pro Gln Ile Gln Thr Ser Gly Thr Val Tyr Lys Leu Asn 50 55 60 Ser Pro Phe Thr Ile Lys Ile Pro Ile Leu Lys Ile His Ser Gly Asp 65 70 75 80 Glu Asn Arg Asp Ser His Ile Met Glu Ile Leu Gly Tyr Pro Asp Ile 85 90 95 Pro Glu Ile Ile Val Val Val Glu Ser Ala Glu Ala Val Gly Glu Thr 100 105 110 Tyr Leu Ile Arg Gly Lys Leu Ser Ile His Gly Phe Thr Arg Asp Phe 115 120 125 Gln Ser Ser Gly Lys Val Glu Pro Asn Gly Val Gly Gln Ile Arg Ile 130 135 140 Phe Gly Lys Val Asn Ile Gln Phe Ser Asp Phe Asn Leu Glu Arg Pro 145 150 155 160 Ser Leu Leu Phe Ile Lys Thr Lys Glu Glu Ile Glu Ile Gly Tyr Asp 165 170 175 Phe Leu Ile Lys Ile 180 33 588 DNA Leptospira interrogans serovar copenhageni CDS (1)...(585) 33 atg gtc aaa aag att ttg aat ctg att ctg ctc ggt gca att gca ttt 48 Met Val Lys Lys Ile Leu Asn Leu Ile Leu Leu Gly Ala Ile Ala Phe 1 5 10 15 tca ttc act ctc tgc tcc tct gct gaa aaa aaa gag gaa tcc gca gct 96 Ser Phe Thr Leu Cys Ser Ser Ala Glu Lys Lys Glu Glu Ser Ala Ala 20 25 30 cct gag cct tca acg caa gag caa tcc gca gct gca aac aga aat gtt 144 Pro Glu Pro Ser Thr Gln Glu Gln Ser Ala Ala Ala Asn Arg Asn Val 35 40 45 gac gtc aat tct ccg gaa gcg atc gca gat tct tta aac gaa aaa cta 192 Asp Val Asn Ser Pro Glu Ala Ile Ala Asp Ser Leu Asn Glu Lys Leu 50 55 60 aaa gat ttc cga tat cca gac ggt tta act cgt cct gga ttt agt tat 240 Lys Asp Phe Arg Tyr Pro Asp Gly Leu Thr Arg Pro Gly Phe Ser Tyr 65 70 75 80 aaa aaa gcg gat gtt acc cct ggt gat ttc agc gag tgg tct aaa aca 288 Lys Lys Ala Asp Val Thr Pro Gly Asp Phe Ser Glu Trp Ser Lys Thr 85 90 95 aac gct cct gta atc aaa gaa ggt ctt gga aaa ctt cca gat agt tac 336 Asn Ala Pro Val Ile Lys Glu Gly Leu Gly Lys Leu Pro Asp Ser Tyr 100 105 110 gct ctt gaa att aca gga cac acc gat gcg atc ggt ccc gaa caa gca 384 Ala Leu Glu Ile Thr Gly His Thr Asp Ala Ile Gly Pro Glu Gln Ala 115 120 125 gaa ggt gct aaa aaa gga aat att ttt tac tct gag ctt cgt gca aat 432 Glu Gly Ala Lys Lys Gly Asn Ile Phe Tyr Ser Glu Leu Arg Ala Asn 130 135 140 gca gtt aaa caa gct tta atc aaa caa ggg att cca gca aat cgt atc 480 Ala Val Lys Gln Ala Leu Ile Lys Gln Gly Ile Pro Ala Asn Arg Ile 145 150 155 160 gtt act aaa ggt gcc ggt tct tcc gag cca gtt tct ggt ctt gat gcg 528 Val Thr Lys Gly Ala Gly Ser Ser Glu Pro Val Ser Gly Leu Asp Ala 165 170 175 aaa gat gct aaa aat aga aga gtc act ttc cgt ttt gcg act tcc gca 576 Lys Asp Ala Lys Asn Arg Arg Val Thr Phe Arg Phe Ala Thr Ser Ala 180 185 190 cca caa caa taa 588 Pro Gln Gln 195 34 195 PRT Leptospira interrogans serovar copenhageni 34 Met Val Lys Lys Ile Leu Asn Leu Ile Leu Leu Gly Ala Ile Ala Phe 1 5 10 15 Ser Phe Thr Leu Cys Ser Ser Ala Glu Lys Lys Glu Glu Ser Ala Ala 20 25 30 Pro Glu Pro Ser Thr Gln Glu Gln Ser Ala Ala Ala Asn Arg Asn Val 35 40 45 Asp Val Asn Ser Pro Glu Ala Ile Ala Asp Ser Leu Asn Glu Lys Leu 50 55 60 Lys Asp Phe Arg Tyr Pro Asp Gly Leu Thr Arg Pro Gly Phe Ser Tyr 65 70 75 80 Lys Lys Ala Asp Val Thr Pro Gly Asp Phe Ser Glu Trp Ser Lys Thr 85 90 95 Asn Ala Pro Val Ile Lys Glu Gly Leu Gly Lys Leu Pro Asp Ser Tyr 100 105 110 Ala Leu Glu Ile Thr Gly His Thr Asp Ala Ile Gly Pro Glu Gln Ala 115 120 125 Glu Gly Ala Lys Lys Gly Asn Ile Phe Tyr Ser Glu Leu Arg Ala Asn 130 135 140 Ala Val Lys Gln Ala Leu Ile Lys Gln Gly Ile Pro Ala Asn Arg Ile 145 150 155 160 Val Thr Lys Gly Ala Gly Ser Ser Glu Pro Val Ser Gly Leu Asp Ala 165 170 175 Lys Asp Ala Lys Asn Arg Arg Val Thr Phe Arg Phe Ala Thr Ser Ala 180 185 190 Pro Gln Gln 195 35 1674 DNA Leptospira interrogans serovar copenhageni CDS (1)...(1671) 35 atg tat tac aaa aag aaa agg aca tta gaa aaa ttt ctc gtt ttc gga 48 Met Tyr Tyr Lys Lys Lys Arg Thr Leu Glu Lys Phe Leu Val Phe Gly 1 5 10 15 acc att cta ctc acg atg att cag cct act tgg agt gag gac ata ctt 96 Thr Ile Leu Leu Thr Met Ile Gln Pro Thr Trp Ser Glu Asp Ile Leu 20 25 30 ccg gaa gaa act gtt tta gaa gag aat aaa aaa tct ccc gtt gaa aat 144 Pro Glu Glu Thr Val Leu Glu Glu Asn Lys Lys Ser Pro Val Glu Asn 35 40 45 tta ggt gac tcc aaa aaa ata ttg aga ctg act tta aaa gac gca gtc 192 Leu Gly Asp Ser Lys Lys Ile Leu Arg Leu Thr Leu Lys Asp Ala Val 50 55 60 aat tat gtt ctt gaa aag aat att aca atc caa aac gct aaa atg gaa 240 Asn Tyr Val Leu Glu Lys Asn Ile Thr Ile Gln Asn Ala Lys Met Glu 65 70 75 80 tat gta aaa gcg gac ggt gga gaa ctt aaa aac gaa tcc caa ttt act 288 Tyr Val Lys Ala Asp Gly Gly Glu Leu Lys Asn Glu Ser Gln Phe Thr 85 90 95 tgg aat cta atc ggt gga att acc gtt ttc agg aca act ctc cct gcc 336 Trp Asn Leu Ile Gly Gly Ile Thr Val Phe Arg Thr Thr Leu Pro Ala 100 105 110 aat aga aat aac atc ttt gcc gga acc aaa caa agc caa gat aaa tta 384 Asn Arg Asn Asn Ile Phe Ala Gly Thr Lys Gln Ser Gln Asp Lys Leu 115 120 125 agc gtc gga att gag aaa aat ttt aga act gga acg tat gca aaa tta 432 Ser Val Gly Ile Glu Lys Asn Phe Arg Thr Gly Thr Tyr Ala Lys Leu 130 135 140 gaa gca agt act act cgt ttt gat acg agc gct ttc gaa aac ccg tcc 480 Glu Ala Ser Thr Thr Arg Phe Asp Thr Ser Ala Phe Glu Asn Pro Ser 145 150 155 160 aca act cct tcc aac tta gcg gcg ctt gca att cct cct tta tat aca 528 Thr Thr Pro Ser Asn Leu Ala Ala Leu Ala Ile Pro Pro Leu Tyr Thr 165 170 175 ggc gct ttg acc atc act tta agc cag gaa atc tta aag tat agt ttt 576 Gly Ala Leu Thr Ile Thr Leu Ser Gln Glu Ile Leu Lys Tyr Ser Phe 180 185 190 gga aaa act cag aaa gaa aga gaa gcc att tta aga caa aat act gta 624 Gly Lys Thr Gln Lys Glu Arg Glu Ala Ile Leu Arg Gln Asn Thr Val 195 200 205 atc aaa aga gaa gaa ttg att tat gta ctt tcg cag ctt gta gca caa 672 Ile Lys Arg Glu Glu Leu Ile Tyr Val Leu Ser Gln Leu Val Ala Gln 210 215 220 aca ttg att caa tat tgg agt tta aat atc tac gac tcg aac gta aaa 720 Thr Leu Ile Gln Tyr Trp Ser Leu Asn Ile Tyr Asp Ser Asn Val Lys 225 230 235 240 acg ctg caa gat tta gaa tcc aat act aga aac atc aga gat ttg acc 768 Thr Leu Gln Asp Leu Glu Ser Asn Thr Arg Asn Ile Arg Asp Leu Thr 245 250 255 gtt aga aaa cga aac tta ggg ctt tcg gaa ggt ttt gaa gtc aat cta 816 Val Arg Lys Arg Asn Leu Gly Leu Ser Glu Gly Phe Glu Val Asn Leu 260 265 270 tgg aat tct att ctt tct caa aca gca ggt aat tta gaa aaa gct aaa 864 Trp Asn Ser Ile Leu Ser Gln Thr Ala Gly Asn Leu Glu Lys Ala Lys 275 280 285 gtg tct cgt aaa gaa gca gaa aga aat tta att cgg att tta aac gcg 912 Val Ser Arg Lys Glu Ala Glu Arg Asn Leu Ile Arg Ile Leu Asn Ala 290 295 300 gat cct tct tct aaa atc gaa ggt gtt act gat ctt caa gaa aac gtt 960 Asp Pro Ser Ser Lys Ile Glu Gly Val Thr Asp Leu Gln Glu Asn Val 305 310 315 320 cct tta gat ttt aac gtg gaa aag gat tat atc tac gca ctt gat cat 1008 Pro Leu Asp Phe Asn Val Glu Lys Asp Tyr Ile Tyr Ala Leu Asp His 325 330 335 aga acc gat cta aaa aat ctt cgc aaa caa agg gaa atc gca gaa tta 1056 Arg Thr Asp Leu Lys Asn Leu Arg Lys Gln Arg Glu Ile Ala Glu Leu 340 345 350 aat ctt aag atc aaa gaa gca gaa gac atg cct tct tta aaa ctt tca 1104 Asn Leu Lys Ile Lys Glu Ala Glu Asp Met Pro Ser Leu Lys Leu Ser 355 360 365 ggg gcc tat tct aca aga gga caa aat att gtt tct cct caa caa aat 1152 Gly Ala Tyr Ser Thr Arg Gly Gln Asn Ile Val Ser Pro Gln Gln Asn 370 375 380 ctc acg gat gga aat aga gga gtc gcc tct ttt aaa tat ccg gaa gca 1200 Leu Thr Asp Gly Asn Arg Gly Val Ala Ser Phe Lys Tyr Pro Glu Ala 385 390 395 400 tac gcg gct ttt caa ttt tct tat cct ctt tgg gat aaa ggg atc aag 1248 Tyr Ala Ala Phe Gln Phe Ser Tyr Pro Leu Trp Asp Lys Gly Ile Lys 405 410 415 gca gat att cga aac gca aaa tta gac gta cag aat cta gaa aaa aaa 1296 Ala Asp Ile Arg Asn Ala Lys Leu Asp Val Gln Asn Leu Glu Lys Lys 420 425 430 gaa gct gag tta aaa ctt tcc atc aaa gaa gaa tta gaa aat cgt tat 1344 Glu Ala Glu Leu Lys Leu Ser Ile Lys Glu Glu Leu Glu Asn Arg Tyr 435 440 445 gct gcc atc gtt gcc gat aaa gat att ttc gaa ggt gct aaa aaa aga 1392 Ala Ala Ile Val Ala Asp Lys Asp Ile Phe Glu Gly Ala Lys Lys Arg 450 455 460 aag gaa gaa gca aat aaa ttc tac aaa ggt ctt tcc gaa cgt ttt cgt 1440 Lys Glu Glu Ala Asn Lys Phe Tyr Lys Gly Leu Ser Glu Arg Phe Arg 465 470 475 480 cag gga aga ttt acc gcg gtc gcg gtt aaa aac gcc tta gac aac gta 1488 Gln Gly Arg Phe Thr Ala Val Ala Val Lys Asn Ala Leu Asp Asn Val 485 490 495 att caa tct gaa tta caa gtt acc cag gca aaa att caa ctg aac ata 1536 Ile Gln Ser Glu Leu Gln Val Thr Gln Ala Lys Ile Gln Leu Asn Ile 500 505 510 gac att ctt cgt tat gaa ttg gca aaa aat cat atc ttc gaa agg ttc 1584 Asp Ile Leu Arg Tyr Glu Leu Ala Lys Asn His Ile Phe Glu Arg Phe 515 520 525 ggc gtg aac gta aat gac atc atc gat cga ctg atg aag atg gtg gat 1632 Gly Val Asn Val Asn Asp Ile Ile Asp Arg Leu Met Lys Met Val Asp 530 535 540 att gca caa tcc aaa tct tct acg gaa act tcc gaa aaa taa 1674 Ile Ala Gln Ser Lys Ser Ser Thr Glu Thr Ser Glu Lys 545 550 555 36 557 PRT Leptospira interrogans serovar copenhageni 36 Met Tyr Tyr Lys Lys Lys Arg Thr Leu Glu Lys Phe Leu Val Phe Gly 1 5 10 15 Thr Ile Leu Leu Thr Met Ile Gln Pro Thr Trp Ser Glu Asp Ile Leu 20 25 30 Pro Glu Glu Thr Val Leu Glu Glu Asn Lys Lys Ser Pro Val Glu Asn 35 40 45 Leu Gly Asp Ser Lys Lys Ile Leu Arg Leu Thr Leu Lys Asp Ala Val 50 55 60 Asn Tyr Val Leu Glu Lys Asn Ile Thr Ile Gln Asn Ala Lys Met Glu 65 70 75 80 Tyr Val Lys Ala Asp Gly Gly Glu Leu Lys Asn Glu Ser Gln Phe Thr 85 90 95 Trp Asn Leu Ile Gly Gly Ile Thr Val Phe Arg Thr Thr Leu Pro Ala 100 105 110 Asn Arg Asn Asn Ile Phe Ala Gly Thr Lys Gln Ser Gln Asp Lys Leu 115 120 125 Ser Val Gly Ile Glu Lys Asn Phe Arg Thr Gly Thr Tyr Ala Lys Leu 130 135 140 Glu Ala Ser Thr Thr Arg Phe Asp Thr Ser Ala Phe Glu Asn Pro Ser 145 150 155 160 Thr Thr Pro Ser Asn Leu Ala Ala Leu Ala Ile Pro Pro Leu Tyr Thr 165 170 175 Gly Ala Leu Thr Ile Thr Leu Ser Gln Glu Ile Leu Lys Tyr Ser Phe 180 185 190 Gly Lys Thr Gln Lys Glu Arg Glu Ala Ile Leu Arg Gln Asn Thr Val 195 200 205 Ile Lys Arg Glu Glu Leu Ile Tyr Val Leu Ser Gln Leu Val Ala Gln 210 215 220 Thr Leu Ile Gln Tyr Trp Ser Leu Asn Ile Tyr Asp Ser Asn Val Lys 225 230 235 240 Thr Leu Gln Asp Leu Glu Ser Asn Thr Arg Asn Ile Arg Asp Leu Thr 245 250 255 Val Arg Lys Arg Asn Leu Gly Leu Ser Glu Gly Phe Glu Val Asn Leu 260 265 270 Trp Asn Ser Ile Leu Ser Gln Thr Ala Gly Asn Leu Glu Lys Ala Lys 275 280 285 Val Ser Arg Lys Glu Ala Glu Arg Asn Leu Ile Arg Ile Leu Asn Ala 290 295 300 Asp Pro Ser Ser Lys Ile Glu Gly Val Thr Asp Leu Gln Glu Asn Val 305 310 315 320 Pro Leu Asp Phe Asn Val Glu Lys Asp Tyr Ile Tyr Ala Leu Asp His 325 330 335 Arg Thr Asp Leu Lys Asn Leu Arg Lys Gln Arg Glu Ile Ala Glu Leu 340 345 350 Asn Leu Lys Ile Lys Glu Ala Glu Asp Met Pro Ser Leu Lys Leu Ser 355 360 365 Gly Ala Tyr Ser Thr Arg Gly Gln Asn Ile Val Ser Pro Gln Gln Asn 370 375 380 Leu Thr Asp Gly Asn Arg Gly Val Ala Ser Phe Lys Tyr Pro Glu Ala 385 390 395 400 Tyr Ala Ala Phe Gln Phe Ser Tyr Pro Leu Trp Asp Lys Gly Ile Lys 405 410 415 Ala Asp Ile Arg Asn Ala Lys Leu Asp Val Gln Asn Leu Glu Lys Lys 420 425 430 Glu Ala Glu Leu Lys Leu Ser Ile Lys Glu Glu Leu Glu Asn Arg Tyr 435 440 445 Ala Ala Ile Val Ala Asp Lys Asp Ile Phe Glu Gly Ala Lys Lys Arg 450 455 460 Lys Glu Glu Ala Asn Lys Phe Tyr Lys Gly Leu Ser Glu Arg Phe Arg 465 470 475 480 Gln Gly Arg Phe Thr Ala Val Ala Val Lys Asn Ala Leu Asp Asn Val 485 490 495 Ile Gln Ser Glu Leu Gln Val Thr Gln Ala Lys Ile Gln Leu Asn Ile 500 505 510 Asp Ile Leu Arg Tyr Glu Leu Ala Lys Asn His Ile Phe Glu Arg Phe 515 520 525 Gly Val Asn Val Asn Asp Ile Ile Asp Arg Leu Met Lys Met Val Asp 530 535 540 Ile Ala Gln Ser Lys Ser Ser Thr Glu Thr Ser Glu Lys 545 550 555 37 480 DNA Leptospira interrogans serovar copenhageni CDS (1)...(477) 27 ttg atc ggt tta agt att gcg att ttg att cga tcc ttt ctt ttt ttt 48 Leu Ile Gly Leu Ser Ile Ala Ile Leu Ile Arg Ser Phe Leu Phe Phe 1 5 10 15 cca ttt acg ttg gaa acc aaa gac atg ctt cct act tat tcc cct gga 96 Pro Phe Thr Leu Glu Thr Lys Asp Met Leu Pro Thr Tyr Ser Pro Gly 20 25 30 aaa aga att tat ttc cat agg ttt gta aat cgt tcc aat ctc tat ctt 144 Lys Arg Ile Tyr Phe His Arg Phe Val Asn Arg Ser Asn Leu Tyr Leu 35 40 45 gga gat tta gtt tta gtc aaa cat cca act caa gaa ggt aag gta gtt 192 Gly Asp Leu Val Leu Val Lys His Pro Thr Gln Glu Gly Lys Val Val 50 55 60 ttt tcc agg atc tcc gga aaa cca gga gac aca gtt caa atg aaa aat 240 Phe Ser Arg Ile Ser Gly Lys Pro Gly Asp Thr Val Gln Met Lys Asn 65 70 75 80 aag atc ttg tat cgt aat aat cat cca gaa gat att tct ggt gtt ggg 288 Lys Ile Leu Tyr Arg Asn Asn His Pro Glu Asp Ile Ser Gly Val Gly 85 90 95 agt ggc ttt aca ctt cag ttc gaa gat aaa cga gga gca ttt ccc tcc 336 Ser Gly Phe Thr Leu Gln Phe Glu Asp Lys Arg Gly Ala Phe Pro Ser 100 105 110 agt ttt tct ggc aga gac aac gga gaa cct ttg att ctt aaa gac cga 384 Ser Phe Ser Gly Arg Asp Asn Gly Glu Pro Leu Ile Leu Lys Asp Arg 115 120 125 gat tat ttt ctt ctc tgc gac aac cga gat tct tgc tcc gac tcc aga 432 Asp Tyr Phe Leu Leu Cys Asp Asn Arg Asp Ser Cys Ser Asp Ser Arg 130 135 140 gat ttt ggt cca att cct ata gaa aac ata tta gga aaa gcg ttc taa 480 Asp Phe Gly Pro Ile Pro Ile Glu Asn Ile Leu Gly Lys Ala Phe 145 150 155 38 159 PRT Leptospira interrogans serovar copenhageni 38 Leu Ile Gly Leu Ser Ile Ala Ile Leu Ile Arg Ser Phe Leu Phe Phe 1 5 10 15 Pro Phe Thr Leu Glu Thr Lys Asp Met Leu Pro Thr Tyr Ser Pro Gly 20 25 30 Lys Arg Ile Tyr Phe His Arg Phe Val Asn Arg Ser Asn Leu Tyr Leu 35 40 45 Gly Asp Leu Val Leu Val Lys His Pro Thr Gln Glu Gly Lys Val Val 50 55 60 Phe Ser Arg Ile Ser Gly Lys Pro Gly Asp Thr Val Gln Met Lys Asn 65 70 75 80 Lys Ile Leu Tyr Arg Asn Asn His Pro Glu Asp Ile Ser Gly Val Gly 85 90 95 Ser Gly Phe Thr Leu Gln Phe Glu Asp Lys Arg Gly Ala Phe Pro Ser 100 105 110 Ser Phe Ser Gly Arg Asp Asn Gly Glu Pro Leu Ile Leu Lys Asp Arg 115 120 125 Asp Tyr Phe Leu Leu Cys Asp Asn Arg Asp Ser Cys Ser Asp Ser Arg 130 135 140 Asp Phe Gly Pro Ile Pro Ile Glu Asn Ile Leu Gly Lys Ala Phe 145 150 155 39 966 DNA Leptospira interrogans serovar copenhageni CDS (1)...(963) 39 atg gtt ttt tcc aga tca acc gat ttg ttt aaa gga atc aat agg acc 48 Met Val Phe Ser Arg Ser Thr Asp Leu Phe Lys Gly Ile Asn Arg Thr 1 5 10 15 gag gaa act atg aaa caa ata gca atc tta acc gcc ctg atc att ttt 96 Glu Glu Thr Met Lys Gln Ile Ala Ile Leu Thr Ala Leu Ile Ile Phe 20 25 30 acg tct tgt gcg tcg gta gag tct aaa cga agc gtc agc gct tct gga 144 Thr Ser Cys Ala Ser Val Glu Ser Lys Arg Ser Val Ser Ala Ser Gly 35 40 45 gat ccg tcg gag att ttt ttt gaa aaa gaa att att ccg atg gat tct 192 Asp Pro Ser Glu Ile Phe Phe Glu Lys Glu Ile Ile Pro Met Asp Ser 50 55 60 aat tca aat ttc gtt tct caa aaa cct gca cgt aga tct ttc gaa gaa 240 Asn Ser Asn Phe Val Ser Gln Lys Pro Ala Arg Arg Ser Phe Glu Glu 65 70 75 80 gaa ttg agt gtt gaa aag tat gca aaa gct caa cca cct gaa aaa acc 288 Glu Leu Ser Val Glu Lys Tyr Ala Lys Ala Gln Pro Pro Glu Lys Thr 85 90 95 aat tct tct gga gat ttt gac gaa gtt gga atg tct tcc tgg tat ggc 336 Asn Ser Ser Gly Asp Phe Asp Glu Val Gly Met Ser Ser Trp Tyr Gly 100 105 110 gca aag ttt cac ggt aaa cca acg gca agc gga gaa aaa ttt gat aaa 384 Ala Lys Phe His Gly Lys Pro Thr Ala Ser Gly Glu Lys Phe Asp Lys 115 120 125 aca aaa cta act gct gca cat cca aca ctt cct tta ggt tcc atc att 432 Thr Lys Leu Thr Ala Ala His Pro Thr Leu Pro Leu Gly Ser Ile Ile 130 135 140 aga gtt caa aat tta gaa aac caa aaa gaa gtt ata gtt cgt gtc aac 480 Arg Val Gln Asn Leu Glu Asn Gln Lys Glu Val Ile Val Arg Val Asn 145 150 155 160 gat aga gga cct ttt gta aag gat aga atc att gat ctt tct gaa aaa 528 Asp Arg Gly Pro Phe Val Lys Asp Arg Ile Ile Asp Leu Ser Glu Lys 165 170 175 gct gca gat act tta gat ttt aaa gat gta ggt att gct aaa gta ggt 576 Ala Ala Asp Thr Leu Asp Phe Lys Asp Val Gly Ile Ala Lys Val Gly 180 185 190 att aaa gta gta aaa cgt gga gga gct gca aac gaa gaa tcc gaa gat 624 Ile Lys Val Val Lys Arg Gly Gly Ala Ala Asn Glu Glu Ser Glu Asp 195 200 205 ctc gaa aat tct gac gat gaa gaa gct ctt tta gaa gat gga aaa cct 672 Leu Glu Asn Ser Asp Asp Glu Glu Ala Leu Leu Glu Asp Gly Lys Pro 210 215 220 gaa aaa cta aat cct caa aaa tcg gat tat caa aac aaa ccg att gcc 720 Glu Lys Leu Asn Pro Gln Lys Ser Asp Tyr Gln Asn Lys Pro Ile Ala 225 230 235 240 ggt gga aag tat atc aaa ggt gct cct aaa gga tat acg gtt caa gta 768 Gly Gly Lys Tyr Ile Lys Gly Ala Pro Lys Gly Tyr Thr Val Gln Val 245 250 255 ggt gtt ttt cgg gaa caa tct aga gct gaa tct tat aaa tct aat ctt 816 Gly Val Phe Arg Glu Gln Ser Arg Ala Glu Ser Tyr Lys Ser Asn Leu 260 265 270 gga caa gaa tac ggt gaa aaa act ttc cta ttt aca aga gat ggt tta 864 Gly Gln Glu Tyr Gly Glu Lys Thr Phe Leu Phe Thr Arg Asp Gly Leu 275 280 285 ttt gta att cag tta ggg gat ttc gca agc aga act gag gcg gaa tcg 912 Phe Val Ile Gln Leu Gly Asp Phe Ala Ser Arg Thr Glu Ala Glu Ser 290 295 300 ttg aaa tcg aaa tta aaa aac gat gga att gac tgt ttc att ccg aaa 960 Leu Lys Ser Lys Leu Lys Asn Asp Gly Ile Asp Cys Phe Ile Pro Lys 305 310 315 320 aaa taa 966 Lys 40 321 PRT Leptospira interrogans serovar copenhageni 40 Met Val Phe Ser Arg Ser Thr Asp Leu Phe Lys Gly Ile Asn Arg Thr 1 5 10 15 Glu Glu Thr Met Lys Gln Ile Ala Ile Leu Thr Ala Leu Ile Ile Phe 20 25 30 Thr Ser Cys Ala Ser Val Glu Ser Lys Arg Ser Val Ser Ala Ser Gly 35 40 45 Asp Pro Ser Glu Ile Phe Phe Glu Lys Glu Ile Ile Pro Met Asp Ser 50 55 60 Asn Ser Asn Phe Val Ser Gln Lys Pro Ala Arg Arg Ser Phe Glu Glu 65 70 75 80 Glu Leu Ser Val Glu Lys Tyr Ala Lys Ala Gln Pro Pro Glu Lys Thr 85 90 95 Asn Ser Ser Gly Asp Phe Asp Glu Val Gly Met Ser Ser Trp Tyr Gly 100 105 110 Ala Lys Phe His Gly Lys Pro Thr Ala Ser Gly Glu Lys Phe Asp Lys 115 120 125 Thr Lys Leu Thr Ala Ala His Pro Thr Leu Pro Leu Gly Ser Ile Ile 130 135 140 Arg Val Gln Asn Leu Glu Asn Gln Lys Glu Val Ile Val Arg Val Asn 145 150 155 160 Asp Arg Gly Pro Phe Val Lys Asp Arg Ile Ile Asp Leu Ser Glu Lys 165 170 175 Ala Ala Asp Thr Leu Asp Phe Lys Asp Val Gly Ile Ala Lys Val Gly 180 185 190 Ile Lys Val Val Lys Arg Gly Gly Ala Ala Asn Glu Glu Ser Glu Asp 195 200 205 Leu Glu Asn Ser Asp Asp Glu Glu Ala Leu Leu Glu Asp Gly Lys Pro 210 215 220 Glu Lys Leu Asn Pro Gln Lys Ser Asp Tyr Gln Asn Lys Pro Ile Ala 225 230 235 240 Gly Gly Lys Tyr Ile Lys Gly Ala Pro Lys Gly Tyr Thr Val Gln Val 245 250 255 Gly Val Phe Arg Glu Gln Ser Arg Ala Glu Ser Tyr Lys Ser Asn Leu 260 265 270 Gly Gln Glu Tyr Gly Glu Lys Thr Phe Leu Phe Thr Arg Asp Gly Leu 275 280 285 Phe Val Ile Gln Leu Gly Asp Phe Ala Ser Arg Thr Glu Ala Glu Ser 290 295 300 Leu Lys Ser Lys Leu Lys Asn Asp Gly Ile Asp Cys Phe Ile Pro Lys 305 310 315 320 Lys 41 1053 DNA Leptospira interrogans serovar copenhageni CDS (1)...(1050) 41 atg gaa cct aat tca gat tca aat cga agg tca aat atg gaa cga gca 48 Met Glu Pro Asn Ser Asp Ser Asn Arg Arg Ser Asn Met Glu Arg Ala 1 5 10 15 att tca aac gaa atg aca cgg cta gaa ctc agt gaa ttt tta tcg gat 96 Ile Ser Asn Glu Met Thr Arg Leu Glu Leu Ser Glu Phe Leu Ser Asp 20 25 30 cca aga tct aga aaa gaa ttt ttt gag ttg atg aaa tta aag aat aaa 144 Pro Arg Ser Arg Lys Glu Phe Phe Glu Leu Met Lys Leu Lys Asn Lys 35 40 45 atc gga cat tta gaa atg aat cta aag tta gga tcc gat gaa aac aaa 192 Ile Gly His Leu Glu Met Asn Leu Lys Leu Gly Ser Asp Glu Asn Lys 50 55 60 agt aga act ttc tat att aga aat tca tta tta gct gct gct tgt gtt 240 Ser Arg Thr Phe Tyr Ile Arg Asn Ser Leu Leu Ala Ala Ala Cys Val 65 70 75 80 ctt ttg ctt tca gct cta gct ttt tat ttc aga ttt ttt tct tcg gaa 288 Leu Leu Leu Ser Ala Leu Ala Phe Tyr Phe Arg Phe Phe Ser Ser Glu 85 90 95 caa aac gaa ttt gaa att aca aaa tca gta act act ggt cag tgt aat 336 Gln Asn Glu Phe Glu Ile Thr Lys Ser Val Thr Thr Gly Gln Cys Asn 100 105 110 gtt tct att aat aaa gaa aac att att ctg aaa tcg ggt aag gat tct 384 Val Ser Ile Asn Lys Glu Asn Ile Ile Leu Lys Ser Gly Lys Asp Ser 115 120 125 tat tgt gat tat aca att tcg gga gaa tta gga cta acg ttg agg att 432 Tyr Cys Asp Tyr Thr Ile Ser Gly Glu Leu Gly Leu Thr Leu Arg Ile 130 135 140 tta cca gaa tcc att ttt tca gct tct aaa aaa gga gat gaa gta aat 480 Leu Pro Glu Ser Ile Phe Ser Ala Ser Lys Lys Gly Asp Glu Val Asn 145 150 155 160 cta agt tta agt tcc gga aaa gtt tta ttc act acg aac aaa aaa aaa 528 Leu Ser Leu Ser Ser Gly Lys Val Leu Phe Thr Thr Asn Lys Lys Lys 165 170 175 ata tct tta aaa att cgg tcg aaa gta gat act tta tct tcc gaa ctt 576 Ile Ser Leu Lys Ile Arg Ser Lys Val Asp Thr Leu Ser Ser Glu Leu 180 185 190 ttg gga aca act ctc gtt ttg atc gca gat caa cat tct aaa aaa tat 624 Leu Gly Thr Thr Leu Val Leu Ile Ala Asp Gln His Ser Lys Lys Tyr 195 200 205 caa att atg gtt ttg gaa gga gct ata cga gtc gat tct aca aaa tca 672 Gln Ile Met Val Leu Glu Gly Ala Ile Arg Val Asp Ser Thr Lys Ser 210 215 220 aaa atg gat att tta cct ggt tat tcg gtt ttg aag gat gga tct tct 720 Lys Met Asp Ile Leu Pro Gly Tyr Ser Val Leu Lys Asp Gly Ser Ser 225 230 235 240 gaa agt tct act caa tcc tct ggg caa gaa gtc gag gtt atg aaa att 768 Glu Ser Ser Thr Gln Ser Ser Gly Gln Glu Val Glu Val Met Lys Ile 245 250 255 gag cca aaa gaa ttt aca aaa tac caa gcg ctt tcg gag aat tct aaa 816 Glu Pro Lys Glu Phe Thr Lys Tyr Gln Ala Leu Ser Glu Asn Ser Lys 260 265 270 aag gtc tta aat gaa aac ttt act cat cac aat cgg gaa acg gat ttt 864 Lys Val Leu Asn Glu Asn Phe Thr His His Asn Arg Glu Thr Asp Phe 275 280 285 tta atc aaa tcc gaa ata gaa gag aat tcg tat cct ata tat cgt atc 912 Leu Ile Lys Ser Glu Ile Glu Glu Asn Ser Tyr Pro Ile Tyr Arg Ile 290 295 300 act ctt aaa aac aaa caa gtt gtt tct gga acg atc gaa gag act gaa 960 Thr Leu Lys Asn Lys Gln Val Val Ser Gly Thr Ile Glu Glu Thr Glu 305 310 315 320 aaa ttt tat cta ctt aaa gat aaa gat ggg aat atc aaa gaa att gaa 1008 Lys Phe Tyr Leu Leu Lys Asp Lys Asp Gly Asn Ile Lys Glu Ile Glu 325 330 335 aaa gag gat ata atc gaa tta gaa ctt gtt caa cca aag aac taa 1053 Lys Glu Asp Ile Ile Glu Leu Glu Leu Val Gln Pro Lys Asn 340 345 350 42 350 PRT Leptospira interrogans serovar copenhageni 42 Met Glu Pro Asn Ser Asp Ser Asn Arg Arg Ser Asn Met Glu Arg Ala 1 5 10 15 Ile Ser Asn Glu Met Thr Arg Leu Glu Leu Ser Glu Phe Leu Ser Asp 20 25 30 Pro Arg Ser Arg Lys Glu Phe Phe Glu Leu Met Lys Leu Lys Asn Lys 35 40 45 Ile Gly His Leu Glu Met Asn Leu Lys Leu Gly Ser Asp Glu Asn Lys 50 55 60 Ser Arg Thr Phe Tyr Ile Arg Asn Ser Leu Leu Ala Ala Ala Cys Val 65 70 75 80 Leu Leu Leu Ser Ala Leu Ala Phe Tyr Phe Arg Phe Phe Ser Ser Glu 85 90 95 Gln Asn Glu Phe Glu Ile Thr Lys Ser Val Thr Thr Gly Gln Cys Asn 100 105 110 Val Ser Ile Asn Lys Glu Asn Ile Ile Leu Lys Ser Gly Lys Asp Ser 115 120 125 Tyr Cys Asp Tyr Thr Ile Ser Gly Glu Leu Gly Leu Thr Leu Arg Ile 130 135 140 Leu Pro Glu Ser Ile Phe Ser Ala Ser Lys Lys Gly Asp Glu Val Asn 145 150 155 160 Leu Ser Leu Ser Ser Gly Lys Val Leu Phe Thr Thr Asn Lys Lys Lys 165 170 175 Ile Ser Leu Lys Ile Arg Ser Lys Val Asp Thr Leu Ser Ser Glu Leu 180 185 190 Leu Gly Thr Thr Leu Val Leu Ile Ala Asp Gln His Ser Lys Lys Tyr 195 200 205 Gln Ile Met Val Leu Glu Gly Ala Ile Arg Val Asp Ser Thr Lys Ser 210 215 220 Lys Met Asp Ile Leu Pro Gly Tyr Ser Val Leu Lys Asp Gly Ser Ser 225 230 235 240 Glu Ser Ser Thr Gln Ser Ser Gly Gln Glu Val Glu Val Met Lys Ile 245 250 255 Glu Pro Lys Glu Phe Thr Lys Tyr Gln Ala Leu Ser Glu Asn Ser Lys 260 265 270 Lys Val Leu Asn Glu Asn Phe Thr His His Asn Arg Glu Thr Asp Phe 275 280 285 Leu Ile Lys Ser Glu Ile Glu Glu Asn Ser Tyr Pro Ile Tyr Arg Ile 290 295 300 Thr Leu Lys Asn Lys Gln Val Val Ser Gly Thr Ile Glu Glu Thr Glu 305 310 315 320 Lys Phe Tyr Leu Leu Lys Asp Lys Asp Gly Asn Ile Lys Glu Ile Glu 325 330 335 Lys Glu Asp Ile Ile Glu Leu Glu Leu Val Gln Pro Lys Asn 340 345 350 43 1074 DNA Leptospira interrogans serovar copenhageni CDS (1)...(1071) 43 ttg ttt tta aaa aaa agg aaa gcg gtt tgt aaa gtt ttg tgt cct ttg 48 Leu Phe Leu Lys Lys Arg Lys Ala Val Cys Lys Val Leu Cys Pro Leu 1 5 10 15 aat tcg ctt gaa gcg aat gat agg ttg tcg aat tct tac ctt atg gaa 96 Asn Ser Leu Glu Ala Asn Asp Arg Leu Ser Asn Ser Tyr Leu Met Glu 20 25 30 aaa gaa aca ctg gaa gac tta gag ttt gcc agg atc aaa ctg gaa act 144 Lys Glu Thr Leu Glu Asp Leu Glu Phe Ala Arg Ile Lys Leu Glu Thr 35 40 45 ctc aaa caa gaa ctg gga aaa gaa att aca gga caa gac gaa gtt att 192 Leu Lys Gln Glu Leu Gly Lys Glu Ile Thr Gly Gln Asp Glu Val Ile 50 55 60 cga aac gta ttg gtt tgt ctg atc tgt caa ggt cat gta ctt tta gaa 240 Arg Asn Val Leu Val Cys Leu Ile Cys Gln Gly His Val Leu Leu Glu 65 70 75 80 ggg atg ccc ggg ctt gca aaa aca cta ctt gca agg tca ctt gca agt 288 Gly Met Pro Gly Leu Ala Lys Thr Leu Leu Ala Arg Ser Leu Ala Ser 85 90 95 gcg ctg gat tta aac ttt aaa aga att caa ttt aca cct gat ctt tta 336 Ala Leu Asp Leu Asn Phe Lys Arg Ile Gln Phe Thr Pro Asp Leu Leu 100 105 110 cca gcc gat ctc gtc gga aca gta gta ttt aat cca aaa acc aca gaa 384 Pro Ala Asp Leu Val Gly Thr Val Val Phe Asn Pro Lys Thr Thr Glu 115 120 125 ttt gaa act aga aag gga cca gtg ttt acc gga gtt tta ctc gcg gac 432 Phe Glu Thr Arg Lys Gly Pro Val Phe Thr Gly Val Leu Leu Ala Asp 130 135 140 gaa att aat aga gct ccg gct aag gtt cag tct gct ctt cta gaa agt 480 Glu Ile Asn Arg Ala Pro Ala Lys Val Gln Ser Ala Leu Leu Glu Ser 145 150 155 160 atg gaa gaa aag acc gtt acg att gga gac aaa acc tat aaa cta gac 528 Met Glu Glu Lys Thr Val Thr Ile Gly Asp Lys Thr Tyr Lys Leu Asp 165 170 175 aaa ccg ttt tta gta atc gca act caa aat cca atc gat cag gac gga 576 Lys Pro Phe Leu Val Ile Ala Thr Gln Asn Pro Ile Asp Gln Asp Gly 180 185 190 act tat cct ctt ccc gaa gct cag atg gac cga ttt ttg atg aag atc 624 Thr Tyr Pro Leu Pro Glu Ala Gln Met Asp Arg Phe Leu Met Lys Ile 195 200 205 aac gta gat tac cca act ttg gaa gag gaa gtt tcc att ttg gat caa 672 Asn Val Asp Tyr Pro Thr Leu Glu Glu Glu Val Ser Ile Leu Asp Gln 210 215 220 cac gga aaa ata agt tcg gca aac gga aag att aaa aaa acc gtt tct 720 His Gly Lys Ile Ser Ser Ala Asn Gly Lys Ile Lys Lys Thr Val Ser 225 230 235 240 tcc tct gaa att tta cga cta tct tct atg ctc gac gaa gta ttt atc 768 Ser Ser Glu Ile Leu Arg Leu Ser Ser Met Leu Asp Glu Val Phe Ile 245 250 255 gaa gaa aaa atc aaa tcc tat att gta cga ttg gtt cga aat aca aga 816 Glu Glu Lys Ile Lys Ser Tyr Ile Val Arg Leu Val Arg Asn Thr Arg 260 265 270 cca gaa gaa aga acc att ccg gaa ctc att ccg tat atc cga cac gga 864 Pro Glu Glu Arg Thr Ile Pro Glu Leu Ile Pro Tyr Ile Arg His Gly 275 280 285 gct tct ccg aga gct tct tta agt ata tta aaa agt tct aaa gca aat 912 Ala Ser Pro Arg Ala Ser Leu Ser Ile Leu Lys Ser Ser Lys Ala Asn 290 295 300 gct ctt ttg agt ggt agg aca tac gta act ccg gaa gac gta aaa acg 960 Ala Leu Leu Ser Gly Arg Thr Tyr Val Thr Pro Glu Asp Val Lys Thr 305 310 315 320 tct ctt gtg gaa ata tta aga cat aga ata ctg ctt acc ttt gag gca 1008 Ser Leu Val Glu Ile Leu Arg His Arg Ile Leu Leu Thr Phe Glu Ala 325 330 335 att tcg gaa gaa ttg aac gta gaa tct ttg atc cga act gtt gtg gag 1056 Ile Ser Glu Glu Leu Asn Val Glu Ser Leu Ile Arg Thr Val Val Glu 340 345 350 gca act ccg gtt cct tag 1074 Ala Thr Pro Val Pro 355 44 357 PRT Leptospira interrogans serovar copenhageni 44 Leu Phe Leu Lys Lys Arg Lys Ala Val Cys Lys Val Leu Cys Pro Leu 1 5 10 15 Asn Ser Leu Glu Ala Asn Asp Arg Leu Ser Asn Ser Tyr Leu Met Glu 20 25 30 Lys Glu Thr Leu Glu Asp Leu Glu Phe Ala Arg Ile Lys Leu Glu Thr 35 40 45 Leu Lys Gln Glu Leu Gly Lys Glu Ile Thr Gly Gln Asp Glu Val Ile 50 55 60 Arg Asn Val Leu Val Cys Leu Ile Cys Gln Gly His Val Leu Leu Glu 65 70 75 80 Gly Met Pro Gly Leu Ala Lys Thr Leu Leu Ala Arg Ser Leu Ala Ser 85 90 95 Ala Leu Asp Leu Asn Phe Lys Arg Ile Gln Phe Thr Pro Asp Leu Leu 100 105 110 Pro Ala Asp Leu Val Gly Thr Val Val Phe Asn Pro Lys Thr Thr Glu 115 120 125 Phe Glu Thr Arg Lys Gly Pro Val Phe Thr Gly Val Leu Leu Ala Asp 130 135 140 Glu Ile Asn Arg Ala Pro Ala Lys Val Gln Ser Ala Leu Leu Glu Ser 145 150 155 160 Met Glu Glu Lys Thr Val Thr Ile Gly Asp Lys Thr Tyr Lys Leu Asp 165 170 175 Lys Pro Phe Leu Val Ile Ala Thr Gln Asn Pro Ile Asp Gln Asp Gly 180 185 190 Thr Tyr Pro Leu Pro Glu Ala Gln Met Asp Arg Phe Leu Met Lys Ile 195 200 205 Asn Val Asp Tyr Pro Thr Leu Glu Glu Glu Val Ser Ile Leu Asp Gln 210 215 220 His Gly Lys Ile Ser Ser Ala Asn Gly Lys Ile Lys Lys Thr Val Ser 225 230 235 240 Ser Ser Glu Ile Leu Arg Leu Ser Ser Met Leu Asp Glu Val Phe Ile 245 250 255 Glu Glu Lys Ile Lys Ser Tyr Ile Val Arg Leu Val Arg Asn Thr Arg 260 265 270 Pro Glu Glu Arg Thr Ile Pro Glu Leu Ile Pro Tyr Ile Arg His Gly 275 280 285 Ala Ser Pro Arg Ala Ser Leu Ser Ile Leu Lys Ser Ser Lys Ala Asn 290 295 300 Ala Leu Leu Ser Gly Arg Thr Tyr Val Thr Pro Glu Asp Val Lys Thr 305 310 315 320 Ser Leu Val Glu Ile Leu Arg His Arg Ile Leu Leu Thr Phe Glu Ala 325 330 335 Ile Ser Glu Glu Leu Asn Val Glu Ser Leu Ile Arg Thr Val Val Glu 340 345 350 Ala Thr Pro Val Pro 355 45 480 DNA Leptospira interrogans serovar copenhageni CDS (1)...(477) 45 atg aaa aaa cat tct atc agt aaa atc att ata act gct tgt tgc att 48 Met Lys Lys His Ser Ile Ser Lys Ile Ile Ile Thr Ala Cys Cys Ile 1 5 10 15 ttt ctt tta aca tac gga tgc aaa caa gat cca gta gat tac aat aat 96 Phe Leu Leu Thr Tyr Gly Cys Lys Gln Asp Pro Val Asp Tyr Asn Asn 20 25 30 aaa atc atg gaa atc atg aac gct tct aca aac gat tta gat gcg tta 144 Lys Ile Met Glu Ile Met Asn Ala Ser Thr Asn Asp Leu Asp Ala Leu 35 40 45 aac gca gcc atg gaa aag gaa gac ctt aca aac gca gaa aat gtt aga 192 Asn Ala Ala Met Glu Lys Glu Asp Leu Thr Asn Ala Glu Asn Val Arg 50 55 60 aaa gct tgg gaa aca aag cta gtt tct tca ctc gat aag ctt aaa gga 240 Lys Ala Trp Glu Thr Lys Leu Val Ser Ser Leu Asp Lys Leu Lys Gly 65 70 75 80 atc agt gat ttt aaa gga gat tcc agt ttt aaa aat gca agc gtc caa 288 Ile Ser Asp Phe Lys Gly Asp Ser Ser Phe Lys Asn Ala Ser Val Gln 85 90 95 gct ctc gaa act tat tta aac ata gta agt aaa gac tac aaa cgt ttg 336 Ala Leu Glu Thr Tyr Leu Asn Ile Val Ser Lys Asp Tyr Lys Arg Leu 100 105 110 atc gaa tta cga gga tta ggt gac aaa gca gac tca aat gaa atc aac 384 Ile Glu Leu Arg Gly Leu Gly Asp Lys Ala Asp Ser Asn Glu Ile Asn 115 120 125 caa gtt ctc aat cgt att aat cag gat ttt gaa aaa gct gta aat act 432 Gln Val Leu Asn Arg Ile Asn Gln Asp Phe Glu Lys Ala Val Asn Thr 130 135 140 ctc aat gct gct tct gat aaa ttt gcg aaa gaa tac gct tct caa taa 480 Leu Asn Ala Ala Ser Asp Lys Phe Ala Lys Glu Tyr Ala Ser Gln 145 150 155 46 159 PRT Leptospira interrogans serovar copenhageni 46 Met Lys Lys His Ser Ile Ser Lys Ile Ile Ile Thr Ala Cys Cys Ile 1 5 10 15 Phe Leu Leu Thr Tyr Gly Cys Lys Gln Asp Pro Val Asp Tyr Asn Asn 20 25 30 Lys Ile Met Glu Ile Met Asn Ala Ser Thr Asn Asp Leu Asp Ala Leu 35 40 45 Asn Ala Ala Met Glu Lys Glu Asp Leu Thr Asn Ala Glu Asn Val Arg 50 55 60 Lys Ala Trp Glu Thr Lys Leu Val Ser Ser Leu Asp Lys Leu Lys Gly 65 70 75 80 Ile Ser Asp Phe Lys Gly Asp Ser Ser Phe Lys Asn Ala Ser Val Gln 85 90 95 Ala Leu Glu Thr Tyr Leu Asn Ile Val Ser Lys Asp Tyr Lys Arg Leu 100 105 110 Ile Glu Leu Arg Gly Leu Gly Asp Lys Ala Asp Ser Asn Glu Ile Asn 115 120 125 Gln Val Leu Asn Arg Ile Asn Gln Asp Phe Glu Lys Ala Val Asn Thr 130 135 140 Leu Asn Ala Ala Ser Asp Lys Phe Ala Lys Glu Tyr Ala Ser Gln 145 150 155 

We claim:
 1. An isolated nucleic acid molecule which encodes a Leptospiral surface protein wherein the Leptospiral surface protein consists of an amino acid sequence selected from the group consisting of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20 and
 22. 2. The isolated nucleic acid molecule of claim 1, consisting of the nucleotide sequence set forth in SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, and
 21. 3. Expression vector comprising the isolated nucleic acid molecule of claim 1, operably linked to a promoter.
 4. Recombinant cell, transformed or transfected with the isolated nucleic acid molecule of claim
 1. 5. Recombinant cell, transformed or transfected with the expression vector of claim
 1. 6. Vaccine comprising the isolated nucleic acid molecule of claim 1, in combination with a pharmaceutically acceptable adjuvant or carrier.
 7. An isolated Leptospiral protein consisting of an amino acid sequence selected from the group consisting of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20 and
 22. 8. Vaccine comprising the isolated Leptspiral protein of claim 7, and a pharmaceutically acceptable adjuvant or carrier.
 9. An isolated antibody which specifically binds to the isolated Leptospiral protein of claim
 7. 10. The isolated antibody of claim 9, wherein said antibody is a monoclonal antibody.
 11. Hybridoma cell line which produces the isolated antibody of claim 10
 12. A method for determining a Leptospiral infection in a subject comprising admixing a sample taken from said subject with the isolated protein of claim 7 and determining binding of antibodies to said protein as a determination of a Leptospiral infection.
 13. The method of claim 12, wherein said protein is bound to a solid phase.
 14. The method of claim 12, further comprising contacting said sample with a labeled antibody which binds to antibodies bound to said protein.
 15. A method for determining a Leptospiral infection in a subject, comprising admixing a sample taken from said subject with the isolated antibody of claim 9, and determining binding of protein in said sample to said antibody as a determination of a Leptospiral infection.
 16. The method of claim 15, wherein said antibody is bound to a solid phase.
 17. The method of claim 15, further comprising contacting said sample with a labeled antibody which binds to protein bound to said isolated antibody. 